Name: rs1419108
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1419108

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:131060995 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.381604 (104535/273936, ALFA)
C=0.286611 (75863/264690, TOPMED)
C=0.300107 (42012/139990, GnomAD) (+ 22 more)
C=0.24155 (19010/78700, PAGE_STUDY)
C=0.44168 (12481/28258, 14KJPN)
C=0.44236 (7414/16760, 8.3KJPN)
C=0.2839 (1818/6404, 1000G_30x)
C=0.2891 (1448/5008, 1000G)
C=0.4007 (1795/4480, Estonian)
C=0.3996 (1540/3854, ALSPAC)
C=0.3878 (1438/3708, TWINSUK)
C=0.3768 (1104/2930, KOREAN)
C=0.3090 (644/2084, HGDP_Stanford)
C=0.2590 (490/1892, HapMap)
C=0.4067 (745/1832, Korea1K)
C=0.409 (408/998, GoNL)
C=0.313 (246/786, PRJEB37584)
C=0.393 (236/600, NorthernSweden)
C=0.227 (113/498, SGDP_PRJ)
C=0.356 (77/216, Qatari)
C=0.354 (75/212, Vietnamese)
C=0.33 (26/78, Ancient Sardinia)
C=0.28 (14/50, Siberian)
C=0.50 (20/40, GENOME_DK)
T=0.50 (20/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	278972	C=0.380493	G=0.000000, T=0.619507
European	Sub	249620	C=0.391563	G=0.000000, T=0.608437
African	Sub	7678	C=0.1261	G=0.0000, T=0.8739
African Others	Sub	294	C=0.102	G=0.000, T=0.898
African American	Sub	7384	C=0.1270	G=0.0000, T=0.8730
Asian	Sub	3642	C=0.3652	G=0.0000, T=0.6348
East Asian	Sub	2906	C=0.3630	G=0.0000, T=0.6370
Other Asian	Sub	736	C=0.374	G=0.000, T=0.626
Latin American 1	Sub	814	C=0.332	G=0.000, T=0.668
Latin American 2	Sub	4228	C=0.2904	G=0.0000, T=0.7096
South Asian	Sub	5172	C=0.3919	G=0.0000, T=0.6081
Other	Sub	7818	C=0.3303	G=0.0000, T=0.6697

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	273936	C=0.381604	G=0.000000, T=0.618396
Allele Frequency Aggregator	European	Sub	246526	C=0.391492	G=0.000000, T=0.608508
Allele Frequency Aggregator	Other	Sub	7018	C=0.3323	G=0.0000, T=0.6677
Allele Frequency Aggregator	African	Sub	6536	C=0.1278	G=0.0000, T=0.8722
Allele Frequency Aggregator	South Asian	Sub	5172	C=0.3919	G=0.0000, T=0.6081
Allele Frequency Aggregator	Latin American 2	Sub	4228	C=0.2904	G=0.0000, T=0.7096
Allele Frequency Aggregator	Asian	Sub	3642	C=0.3652	G=0.0000, T=0.6348
Allele Frequency Aggregator	Latin American 1	Sub	814	C=0.332	G=0.000, T=0.668
TopMed	Global	Study-wide	264690	C=0.286611	T=0.713389
gnomAD - Genomes	Global	Study-wide	139990	C=0.300107	T=0.699893
gnomAD - Genomes	European	Sub	75802	C=0.39387	T=0.60613
gnomAD - Genomes	African	Sub	41970	C=0.12954	T=0.87046
gnomAD - Genomes	American	Sub	13630	C=0.27667	T=0.72333
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.3866	T=0.6134
gnomAD - Genomes	East Asian	Sub	3112	C=0.3242	T=0.6758
gnomAD - Genomes	Other	Sub	2152	C=0.3039	T=0.6961
The PAGE Study	Global	Study-wide	78700	C=0.24155	T=0.75845
The PAGE Study	AfricanAmerican	Sub	32516	C=0.13753	T=0.86247
The PAGE Study	Mexican	Sub	10808	C=0.28571	T=0.71429
The PAGE Study	Asian	Sub	8318	C=0.4146	T=0.5854
The PAGE Study	PuertoRican	Sub	7918	C=0.2693	T=0.7307
The PAGE Study	NativeHawaiian	Sub	4534	C=0.3902	T=0.6098
The PAGE Study	Cuban	Sub	4230	C=0.3161	T=0.6839
The PAGE Study	Dominican	Sub	3828	C=0.2223	T=0.7777
The PAGE Study	CentralAmerican	Sub	2450	C=0.2359	T=0.7641
The PAGE Study	SouthAmerican	Sub	1982	C=0.2856	T=0.7144
The PAGE Study	NativeAmerican	Sub	1260	C=0.3389	T=0.6611
The PAGE Study	SouthAsian	Sub	856	C=0.398	T=0.602
14KJPN	JAPANESE	Study-wide	28258	C=0.44168	T=0.55832
8.3KJPN	JAPANESE	Study-wide	16760	C=0.44236	T=0.55764
1000Genomes_30x	Global	Study-wide	6404	C=0.2839	T=0.7161
1000Genomes_30x	African	Sub	1786	C=0.0655	T=0.9345
1000Genomes_30x	Europe	Sub	1266	C=0.3870	T=0.6130
1000Genomes_30x	South Asian	Sub	1202	C=0.4118	T=0.5882
1000Genomes_30x	East Asian	Sub	1170	C=0.3556	T=0.6444
1000Genomes_30x	American	Sub	980	C=0.306	T=0.694
1000Genomes	Global	Study-wide	5008	C=0.2891	T=0.7109
1000Genomes	African	Sub	1322	C=0.0688	T=0.9312
1000Genomes	East Asian	Sub	1008	C=0.3591	T=0.6409
1000Genomes	Europe	Sub	1006	C=0.3867	T=0.6133
1000Genomes	South Asian	Sub	978	C=0.401	T=0.599
1000Genomes	American	Sub	694	C=0.308	T=0.692
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.4007	T=0.5993
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.3996	T=0.6004
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.3878	T=0.6122
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.3768	A=0.0000, T=0.6232
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.3090	T=0.6910
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.313	T=0.687
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.413	T=0.587
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.369	T=0.631
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.372	T=0.628
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.054	T=0.946
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.227	T=0.773
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.22	T=0.78
HapMap	Global	Study-wide	1892	C=0.2590	T=0.7410
HapMap	American	Sub	770	C=0.312	T=0.688
HapMap	African	Sub	692	C=0.123	T=0.877
HapMap	Asian	Sub	254	C=0.374	T=0.626
HapMap	Europe	Sub	176	C=0.398	T=0.602
Korean Genome Project	KOREAN	Study-wide	1832	C=0.4067	T=0.5933
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.409	T=0.591
CNV burdens in cranial meningiomas	Global	Study-wide	786	C=0.313	T=0.687
CNV burdens in cranial meningiomas	CRM	Sub	786	C=0.313	T=0.687
Northern Sweden	ACPOP	Study-wide	600	C=0.393	T=0.607
SGDP_PRJ	Global	Study-wide	498	C=0.227	T=0.773
Qatari	Global	Study-wide	216	C=0.356	T=0.644
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.354	T=0.646
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	78	C=0.33	T=0.67
Siberian	Global	Study-wide	50	C=0.28	T=0.72
The Danish reference pan genome	Danish	Study-wide	40	C=0.50	T=0.50

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.131060995C>A
GRCh38.p14 chr 10	NC_000010.11:g.131060995C>G
GRCh38.p14 chr 10	NC_000010.11:g.131060995C>T
GRCh37.p13 chr 10	NC_000010.10:g.132859258C>A
GRCh37.p13 chr 10	NC_000010.10:g.132859258C>G
GRCh37.p13 chr 10	NC_000010.10:g.132859258C>T

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	C=	A	G	T
GRCh38.p14 chr 10	NC_000010.11:g.131060995=	NC_000010.11:g.131060995C>A	NC_000010.11:g.131060995C>G	NC_000010.11:g.131060995C>T
GRCh37.p13 chr 10	NC_000010.10:g.132859258=	NC_000010.10:g.132859258C>A	NC_000010.10:g.132859258C>G	NC_000010.10:g.132859258C>T

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

144 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2223132	Oct 23, 2000 (88)
2	TSC-CSHL	ss5480706	Oct 08, 2002 (108)
3	SC_JCM	ss5723858	Feb 20, 2003 (111)
4	WI_SSAHASNP	ss12089895	Jul 11, 2003 (116)
5	SC_SNP	ss15472001	Feb 27, 2004 (120)
6	CSHL-HAPMAP	ss16486625	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss19172508	Feb 27, 2004 (120)
8	CSHL-HAPMAP	ss19887711	Feb 27, 2004 (120)
9	SSAHASNP	ss20614317	Apr 05, 2004 (123)
10	PERLEGEN	ss24085490	Sep 20, 2004 (123)
11	ABI	ss38514991	Mar 15, 2006 (126)
12	ILLUMINA	ss66671718	Dec 02, 2006 (127)
13	ILLUMINA	ss67099920	Dec 02, 2006 (127)
14	ILLUMINA	ss67435149	Dec 02, 2006 (127)
15	ILLUMINA	ss70431050	May 18, 2007 (127)
16	ILLUMINA	ss70615772	May 24, 2008 (130)
17	ILLUMINA	ss71163766	May 18, 2007 (127)
18	ILLUMINA	ss75578385	Dec 07, 2007 (129)
19	AFFY	ss76701220	Dec 07, 2007 (129)
20	HGSV	ss78899156	Dec 07, 2007 (129)
21	HGSV	ss82924533	Dec 14, 2007 (130)
22	KRIBB_YJKIM	ss83764563	Dec 14, 2007 (130)
23	HGSV	ss85147142	Dec 14, 2007 (130)
24	BCMHGSC_JDW	ss88414067	Mar 23, 2008 (129)
25	BGI	ss102927786	Feb 20, 2009 (130)
26	1000GENOMES	ss109880505	Jan 24, 2009 (130)
27	1000GENOMES	ss114043728	Jan 25, 2009 (130)
28	ILLUMINA-UK	ss119332444	Feb 15, 2009 (130)
29	ILLUMINA	ss121688352	Dec 01, 2009 (131)
30	ENSEMBL	ss131860080	Dec 01, 2009 (131)
31	ENSEMBL	ss132200179	Dec 01, 2009 (131)
32	ILLUMINA	ss153425244	Dec 01, 2009 (131)
33	GMI	ss155760638	Dec 01, 2009 (131)
34	ILLUMINA	ss159267535	Dec 01, 2009 (131)
35	COMPLETE_GENOMICS	ss168817386	Jul 04, 2010 (132)
36	ILLUMINA	ss170488023	Jul 04, 2010 (132)
37	COMPLETE_GENOMICS	ss171407539	Jul 04, 2010 (132)
38	ILLUMINA	ss172486992	Jul 04, 2010 (132)
39	BUSHMAN	ss202216003	Jul 04, 2010 (132)
40	BCM-HGSC-SUB	ss207005752	Jul 04, 2010 (132)
41	1000GENOMES	ss225029341	Jul 14, 2010 (132)
42	1000GENOMES	ss235398321	Jul 15, 2010 (132)
43	1000GENOMES	ss242063148	Jul 15, 2010 (132)
44	BL	ss254738807	May 09, 2011 (134)
45	GMI	ss280836330	May 04, 2012 (137)
46	GMI	ss286293229	Apr 25, 2013 (138)
47	PJP	ss290967121	May 09, 2011 (134)
48	ILLUMINA	ss479965819	May 04, 2012 (137)
49	ILLUMINA	ss479974357	May 04, 2012 (137)
50	ILLUMINA	ss484781165	May 04, 2012 (137)
51	ILLUMINA	ss536868429	Sep 08, 2015 (146)
52	TISHKOFF	ss562310987	Apr 25, 2013 (138)
53	SSMP	ss657595488	Apr 25, 2013 (138)
54	ILLUMINA	ss778805775	Sep 08, 2015 (146)
55	ILLUMINA	ss782837255	Sep 08, 2015 (146)
56	ILLUMINA	ss783801971	Sep 08, 2015 (146)
57	ILLUMINA	ss825400324	Apr 01, 2015 (144)
58	ILLUMINA	ss832090868	Sep 08, 2015 (146)
59	ILLUMINA	ss832779728	Jul 13, 2019 (153)
60	ILLUMINA	ss834265985	Sep 08, 2015 (146)
61	EVA-GONL	ss988085754	Aug 21, 2014 (142)
62	JMKIDD_LAB	ss1077420166	Aug 21, 2014 (142)
63	1000GENOMES	ss1339672168	Aug 21, 2014 (142)
64	DDI	ss1426494559	Apr 01, 2015 (144)
65	EVA_GENOME_DK	ss1575453991	Apr 01, 2015 (144)
66	EVA_DECODE	ss1597766294	Apr 01, 2015 (144)
67	EVA_UK10K_ALSPAC	ss1625768773	Apr 01, 2015 (144)
68	EVA_UK10K_TWINSUK	ss1668762806	Apr 01, 2015 (144)
69	EVA_SVP	ss1713224724	Apr 01, 2015 (144)
70	ILLUMINA	ss1751956490	Sep 08, 2015 (146)
71	HAMMER_LAB	ss1806641158	Sep 08, 2015 (146)
72	WEILL_CORNELL_DGM	ss1931442536	Feb 12, 2016 (147)
73	ILLUMINA	ss1946297344	Feb 12, 2016 (147)
74	ILLUMINA	ss1959309254	Feb 12, 2016 (147)
75	GENOMED	ss1967264675	Jul 19, 2016 (147)
76	JJLAB	ss2026462855	Sep 14, 2016 (149)
77	USC_VALOUEV	ss2154743252	Dec 20, 2016 (150)
78	HUMAN_LONGEVITY	ss2179334109	Dec 20, 2016 (150)
79	SYSTEMSBIOZJU	ss2627700942	Nov 08, 2017 (151)
80	ILLUMINA	ss2632785254	Nov 08, 2017 (151)
81	GRF	ss2699007691	Nov 08, 2017 (151)
82	ILLUMINA	ss2710725749	Nov 08, 2017 (151)
83	GNOMAD	ss2895065378	Nov 08, 2017 (151)
84	SWEGEN	ss3007395706	Nov 08, 2017 (151)
85	ILLUMINA	ss3021291479	Nov 08, 2017 (151)
86	BIOINF_KMB_FNS_UNIBA	ss3027023505	Nov 08, 2017 (151)
87	CSHL	ss3349387517	Nov 08, 2017 (151)
88	ILLUMINA	ss3625592352	Oct 12, 2018 (152)
89	ILLUMINA	ss3626572401	Oct 12, 2018 (152)
90	ILLUMINA	ss3630806242	Oct 12, 2018 (152)
91	ILLUMINA	ss3632971228	Oct 12, 2018 (152)
92	ILLUMINA	ss3633669400	Oct 12, 2018 (152)
93	ILLUMINA	ss3634432460	Oct 12, 2018 (152)
94	ILLUMINA	ss3635361401	Oct 12, 2018 (152)
95	ILLUMINA	ss3637112172	Oct 12, 2018 (152)
96	ILLUMINA	ss3637883616	Oct 12, 2018 (152)
97	ILLUMINA	ss3638957400	Oct 12, 2018 (152)
98	ILLUMINA	ss3639478974	Oct 12, 2018 (152)
99	ILLUMINA	ss3640139801	Oct 12, 2018 (152)
100	ILLUMINA	ss3642884031	Oct 12, 2018 (152)
101	ILLUMINA	ss3644550125	Oct 12, 2018 (152)
102	URBANLAB	ss3649503159	Oct 12, 2018 (152)
103	ILLUMINA	ss3651651597	Oct 12, 2018 (152)
104	EGCUT_WGS	ss3674817758	Jul 13, 2019 (153)
105	EVA_DECODE	ss3690988870	Jul 13, 2019 (153)
106	ILLUMINA	ss3725203247	Jul 13, 2019 (153)
107	ACPOP	ss3737815336	Jul 13, 2019 (153)
108	ILLUMINA	ss3744078815	Jul 13, 2019 (153)
109	ILLUMINA	ss3744733408	Jul 13, 2019 (153)
110	EVA	ss3748801574	Jul 13, 2019 (153)
111	PAGE_CC	ss3771594609	Jul 13, 2019 (153)
112	ILLUMINA	ss3772233619	Jul 13, 2019 (153)
113	PACBIO	ss3786830799	Jul 13, 2019 (153)
114	PACBIO	ss3791987371	Jul 13, 2019 (153)
115	PACBIO	ss3796869561	Jul 13, 2019 (153)
116	KHV_HUMAN_GENOMES	ss3814153710	Jul 13, 2019 (153)
117	EVA	ss3832415362	Apr 26, 2020 (154)
118	EVA	ss3839749969	Apr 26, 2020 (154)
119	EVA	ss3845225661	Apr 26, 2020 (154)
120	HGDP	ss3847405595	Apr 26, 2020 (154)
121	SGDP_PRJ	ss3875377181	Apr 26, 2020 (154)
122	KRGDB	ss3923573495	Apr 26, 2020 (154)
123	KOGIC	ss3968979816	Apr 26, 2020 (154)
124	EVA	ss3984643669	Apr 26, 2021 (155)
125	EVA	ss3985511455	Apr 26, 2021 (155)
126	TOPMED	ss4871623351	Apr 26, 2021 (155)
127	TOMMO_GENOMICS	ss5200153700	Apr 26, 2021 (155)
128	1000G_HIGH_COVERAGE	ss5286000729	Oct 16, 2022 (156)
129	EVA	ss5315517106	Oct 16, 2022 (156)
130	EVA	ss5397027767	Oct 16, 2022 (156)
131	HUGCELL_USP	ss5481372084	Oct 16, 2022 (156)
132	EVA	ss5510218363	Oct 16, 2022 (156)
133	1000G_HIGH_COVERAGE	ss5580944749	Oct 16, 2022 (156)
134	SANFORD_IMAGENETICS	ss5624263696	Oct 16, 2022 (156)
135	SANFORD_IMAGENETICS	ss5650403223	Oct 16, 2022 (156)
136	TOMMO_GENOMICS	ss5746731654	Oct 16, 2022 (156)
137	YY_MCH	ss5812021968	Oct 16, 2022 (156)
138	EVA	ss5825171784	Oct 16, 2022 (156)
139	EVA	ss5847383626	Oct 16, 2022 (156)
140	EVA	ss5847615985	Oct 16, 2022 (156)
141	EVA	ss5849811460	Oct 16, 2022 (156)
142	EVA	ss5881152567	Oct 16, 2022 (156)
143	EVA	ss5941717471	Oct 16, 2022 (156)
144	EVA	ss5979344626	Oct 16, 2022 (156)
145	1000Genomes	NC_000010.10 - 132859258	Oct 12, 2018 (152)
146	1000Genomes_30x	NC_000010.11 - 131060995	Oct 16, 2022 (156)
147	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 132859258	Oct 12, 2018 (152)
148	Genetic variation in the Estonian population	NC_000010.10 - 132859258	Oct 12, 2018 (152)
149	The Danish reference pan genome	NC_000010.10 - 132859258	Apr 26, 2020 (154)
150	gnomAD - Genomes	NC_000010.11 - 131060995	Apr 26, 2021 (155)
151	Genome of the Netherlands Release 5	NC_000010.10 - 132859258	Apr 26, 2020 (154)
152	HGDP-CEPH-db Supplement 1	NC_000010.9 - 132749248	Apr 26, 2020 (154)
153	HapMap	NC_000010.11 - 131060995	Apr 26, 2020 (154)
154	KOREAN population from KRGDB	NC_000010.10 - 132859258	Apr 26, 2020 (154)
155	Korean Genome Project	NC_000010.11 - 131060995	Apr 26, 2020 (154)
156	Northern Sweden	NC_000010.10 - 132859258	Jul 13, 2019 (153)
157	The PAGE Study	NC_000010.11 - 131060995	Jul 13, 2019 (153)
158	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 132859258	Apr 26, 2021 (155)
159	CNV burdens in cranial meningiomas	NC_000010.10 - 132859258	Apr 26, 2021 (155)
160	Qatari	NC_000010.10 - 132859258	Apr 26, 2020 (154)
161	SGDP_PRJ	NC_000010.10 - 132859258	Apr 26, 2020 (154)
162	Siberian	NC_000010.10 - 132859258	Apr 26, 2020 (154)
163	8.3KJPN	NC_000010.10 - 132859258	Apr 26, 2021 (155)
164	14KJPN	NC_000010.11 - 131060995	Oct 16, 2022 (156)
165	TopMed	NC_000010.11 - 131060995	Apr 26, 2021 (155)
166	UK 10K study - Twins	NC_000010.10 - 132859258	Oct 12, 2018 (152)
167	A Vietnamese Genetic Variation Database	NC_000010.10 - 132859258	Jul 13, 2019 (153)
168	ALFA	NC_000010.11 - 131060995	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs12761230	Sep 24, 2004 (123)
rs16911624	Oct 08, 2004 (123)
rs57755079	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
30750889, ss3923573495	NC_000010.10:132859257:C:A	NC_000010.11:131060994:C:A	(self)
7078687906	NC_000010.11:131060994:C:G	NC_000010.11:131060994:C:G	(self)
ss78899156, ss82924533, ss85147142, ss3638957400, ss3639478974	NC_000010.8:132749247:C:T	NC_000010.11:131060994:C:T	(self)
83487, ss88414067, ss109880505, ss114043728, ss119332444, ss168817386, ss171407539, ss202216003, ss207005752, ss254738807, ss280836330, ss286293229, ss290967121, ss479965819, ss825400324, ss1597766294, ss1713224724, ss3642884031, ss3847405595	NC_000010.9:132749247:C:T	NC_000010.11:131060994:C:T	(self)
52140061, 28973926, 20556006, 2393265, 12913591, 30750889, 11100201, 737382, 193142, 13484466, 27394161, 7259606, 58123007, 28973926, 6431299, ss225029341, ss235398321, ss242063148, ss479974357, ss484781165, ss536868429, ss562310987, ss657595488, ss778805775, ss782837255, ss783801971, ss832090868, ss832779728, ss834265985, ss988085754, ss1077420166, ss1339672168, ss1426494559, ss1575453991, ss1625768773, ss1668762806, ss1751956490, ss1806641158, ss1931442536, ss1946297344, ss1959309254, ss1967264675, ss2026462855, ss2154743252, ss2627700942, ss2632785254, ss2699007691, ss2710725749, ss2895065378, ss3007395706, ss3021291479, ss3349387517, ss3625592352, ss3626572401, ss3630806242, ss3632971228, ss3633669400, ss3634432460, ss3635361401, ss3637112172, ss3637883616, ss3640139801, ss3644550125, ss3651651597, ss3674817758, ss3737815336, ss3744078815, ss3744733408, ss3748801574, ss3772233619, ss3786830799, ss3791987371, ss3796869561, ss3832415362, ss3839749969, ss3875377181, ss3923573495, ss3984643669, ss3985511455, ss5200153700, ss5315517106, ss5397027767, ss5510218363, ss5624263696, ss5650403223, ss5825171784, ss5847383626, ss5847615985, ss5941717471, ss5979344626	NC_000010.10:132859257:C:T	NC_000010.11:131060994:C:T	(self)
68470684, 368254234, 527276, 25357817, 816078, 80568758, 87169006, 7078687906, ss2179334109, ss3027023505, ss3649503159, ss3690988870, ss3725203247, ss3771594609, ss3814153710, ss3845225661, ss3968979816, ss4871623351, ss5286000729, ss5481372084, ss5580944749, ss5746731654, ss5812021968, ss5849811460, ss5881152567	NC_000010.11:131060994:C:T	NC_000010.11:131060994:C:T	(self)
ss12089895	NT_008818.14:4081762:C:T	NC_000010.11:131060994:C:T	(self)
ss15472001, ss16486625, ss19172508, ss19887711, ss20614317	NT_008818.15:4093188:C:T	NC_000010.11:131060994:C:T	(self)
ss2223132, ss5480706, ss5723858, ss24085490, ss38514991, ss66671718, ss67099920, ss67435149, ss70431050, ss70615772, ss71163766, ss75578385, ss76701220, ss83764563, ss102927786, ss121688352, ss131860080, ss132200179, ss153425244, ss155760638, ss159267535, ss170488023, ss172486992	NT_008818.16:4093188:C:T	NC_000010.11:131060994:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1419108

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1419108