Name: rs6532814
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.

rs6532814

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:99252811 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.372099 (98491/264690, TOPMED)
C=0.453056 (92911/205076, GENOGRAPHIC)
C=0.379934 (53149/139890, GnomAD) (+ 21 more)
C=0.42405 (34159/80554, ALFA)
C=0.09668 (2732/28258, 14KJPN)
C=0.09308 (1560/16760, 8.3KJPN)
C=0.2798 (1792/6404, 1000G_30x)
C=0.2746 (1375/5008, 1000G)
C=0.4442 (1990/4480, Estonian)
C=0.4665 (1798/3854, ALSPAC)
C=0.4817 (1786/3708, TWINSUK)
C=0.1393 (407/2922, KOREAN)
C=0.3503 (730/2084, HGDP_Stanford)
C=0.2563 (485/1892, HapMap)
C=0.3882 (441/1136, Daghestan)
C=0.451 (450/998, GoNL)
C=0.487 (292/600, NorthernSweden)
T=0.389 (115/296, SGDP_PRJ)
C=0.361 (78/216, Qatari)
C=0.074 (16/216, Vietnamese)
T=0.50 (32/64, Ancient Sardinia)
C=0.50 (32/64, Ancient Sardinia)
T=0.29 (12/42, Siberian)
C=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC100507053 : Intron Variant
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	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	80646	T=0.57587	C=0.42413	0.3406	0.18885	0.47055	29
European	Sub	65046	T=0.53424	C=0.46576	0.284445	0.21597	0.499585	0
African	Sub	7162	T=0.8228	C=0.1772	0.676347	0.030718	0.292935	0
African Others	Sub	254	T=0.894	C=0.106	0.811024	0.023622	0.165354	1
African American	Sub	6908	T=0.8202	C=0.1798	0.671395	0.030979	0.297626	0
Asian	Sub	192	T=0.901	C=0.099	0.8125	0.010417	0.177083	0
East Asian	Sub	150	T=0.927	C=0.073	0.866667	0.013333	0.12	1
Other Asian	Sub	42	T=0.81	C=0.19	0.619048	0.0	0.380952	1
Latin American 1	Sub	254	T=0.583	C=0.417	0.354331	0.188976	0.456693	0
Latin American 2	Sub	1232	T=0.5032	C=0.4968	0.253247	0.246753	0.5	0
South Asian	Sub	4958	T=0.7670	C=0.2330	0.592578	0.058491	0.348931	1
Other	Sub	1802	T=0.5855	C=0.4145	0.347392	0.176471	0.476138	0

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.627901	C=0.372099
Genographic Project	Global	Study-wide	205076	T=0.546944	C=0.453056
gnomAD - Genomes	Global	Study-wide	139890	T=0.620066	C=0.379934
gnomAD - Genomes	European	Sub	75802	T=0.53186	C=0.46814
gnomAD - Genomes	African	Sub	41914	T=0.81567	C=0.18433
gnomAD - Genomes	American	Sub	13588	T=0.49639	C=0.50361
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	T=0.4524	C=0.5476
gnomAD - Genomes	East Asian	Sub	3122	T=0.8728	C=0.1272
gnomAD - Genomes	Other	Sub	2146	T=0.5899	C=0.4101
Allele Frequency Aggregator	Total	Global	80554	T=0.57595	C=0.42405
Allele Frequency Aggregator	European	Sub	64972	T=0.53428	C=0.46572
Allele Frequency Aggregator	African	Sub	7162	T=0.8228	C=0.1772
Allele Frequency Aggregator	South Asian	Sub	4958	T=0.7670	C=0.2330
Allele Frequency Aggregator	Other	Sub	1784	T=0.5858	C=0.4142
Allele Frequency Aggregator	Latin American 2	Sub	1232	T=0.5032	C=0.4968
Allele Frequency Aggregator	Latin American 1	Sub	254	T=0.583	C=0.417
Allele Frequency Aggregator	Asian	Sub	192	T=0.901	C=0.099
14KJPN	JAPANESE	Study-wide	28258	T=0.90332	C=0.09668
8.3KJPN	JAPANESE	Study-wide	16760	T=0.90692	C=0.09308
1000Genomes_30x	Global	Study-wide	6404	T=0.7202	C=0.2798
1000Genomes_30x	African	Sub	1786	T=0.8617	C=0.1383
1000Genomes_30x	Europe	Sub	1266	T=0.5039	C=0.4961
1000Genomes_30x	South Asian	Sub	1202	T=0.8270	C=0.1730
1000Genomes_30x	East Asian	Sub	1170	T=0.8667	C=0.1333
1000Genomes_30x	American	Sub	980	T=0.436	C=0.564
1000Genomes	Global	Study-wide	5008	T=0.7254	C=0.2746
1000Genomes	African	Sub	1322	T=0.8525	C=0.1475
1000Genomes	East Asian	Sub	1008	T=0.8750	C=0.1250
1000Genomes	Europe	Sub	1006	T=0.5040	C=0.4960
1000Genomes	South Asian	Sub	978	T=0.830	C=0.170
1000Genomes	American	Sub	694	T=0.439	C=0.561
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.5558	C=0.4442
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.5335	C=0.4665
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5183	C=0.4817
KOREAN population from KRGDB	KOREAN	Study-wide	2922	T=0.8607	C=0.1393
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.6497	C=0.3503
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.768	C=0.232
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.645	C=0.355
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.623	C=0.377
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.531	C=0.469
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.806	C=0.194
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.444	C=0.556
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.65	C=0.35
HapMap	Global	Study-wide	1892	T=0.7437	C=0.2563
HapMap	American	Sub	770	T=0.692	C=0.308
HapMap	African	Sub	692	T=0.818	C=0.182
HapMap	Asian	Sub	254	T=0.866	C=0.134
HapMap	Europe	Sub	176	T=0.500	C=0.500
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	T=0.6118	C=0.3882
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	T=0.597	C=0.403
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.569	C=0.431
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.656	C=0.344
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.491	C=0.509
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.83	C=0.17
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.67	C=0.33
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.549	C=0.451
Northern Sweden	ACPOP	Study-wide	600	T=0.513	C=0.487
SGDP_PRJ	Global	Study-wide	296	T=0.389	C=0.611
Qatari	Global	Study-wide	216	T=0.639	C=0.361
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.926	C=0.074
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	64	T=0.50	C=0.50
Siberian	Global	Study-wide	42	T=0.29	C=0.71
The Danish reference pan genome	Danish	Study-wide	40	T=0.62	C=0.38

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 4	NC_000004.12:g.99252811T>C
GRCh37.p13 chr 4	NC_000004.11:g.100173968T>C

Gene: LOC100507053, uncharacterized LOC100507053 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC100507053 transcript	NR_037884.1:n.	N/A	Intron Variant

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	T=	C
GRCh38.p14 chr 4	NC_000004.12:g.99252811=	NC_000004.12:g.99252811T>C
GRCh37.p13 chr 4	NC_000004.11:g.100173968=	NC_000004.11:g.100173968T>C

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#.

96 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10107056	Jul 11, 2003 (116)
2	WI_SSAHASNP	ss11617566	Jul 11, 2003 (116)
3	CSHL-HAPMAP	ss19594470	Feb 27, 2004 (120)
4	ABI	ss44582612	Mar 13, 2006 (126)
5	PERLEGEN	ss46543406	Mar 13, 2006 (126)
6	ILLUMINA	ss66622886	Nov 30, 2006 (127)
7	ILLUMINA	ss67467634	Nov 30, 2006 (127)
8	ILLUMINA	ss67822129	Nov 30, 2006 (127)
9	ILLUMINA	ss70870953	May 25, 2008 (130)
10	ILLUMINA	ss71459814	May 17, 2007 (127)
11	ILLUMINA	ss75451567	Dec 06, 2007 (129)
12	ILLUMINA	ss79224490	Dec 15, 2007 (130)
13	KRIBB_YJKIM	ss84497085	Dec 15, 2007 (130)
14	HUMANGENOME_JCVI	ss98986803	Feb 05, 2009 (130)
15	1000GENOMES	ss108170951	Jan 23, 2009 (130)
16	ILLUMINA-UK	ss117113681	Feb 14, 2009 (130)
17	ILLUMINA	ss122562356	Dec 01, 2009 (131)
18	ENSEMBL	ss135207887	Dec 01, 2009 (131)
19	ILLUMINA	ss154366184	Dec 01, 2009 (131)
20	ILLUMINA	ss159542350	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss162380177	Jul 04, 2010 (132)
22	ILLUMINA	ss172143140	Jul 04, 2010 (132)
23	ILLUMINA	ss174026830	Jul 04, 2010 (132)
24	1000GENOMES	ss221098764	Jul 14, 2010 (132)
25	1000GENOMES	ss232515111	Jul 14, 2010 (132)
26	1000GENOMES	ss239780123	Jul 15, 2010 (132)
27	GMI	ss277844404	May 04, 2012 (137)
28	PJP	ss293147506	May 09, 2011 (134)
29	ILLUMINA	ss537360807	Sep 08, 2015 (146)
30	TISHKOFF	ss557721165	Apr 25, 2013 (138)
31	SSMP	ss651525721	Apr 25, 2013 (138)
32	ILLUMINA	ss825555008	Jul 19, 2016 (147)
33	ILLUMINA	ss833053552	Aug 21, 2014 (142)
34	ILLUMINA	ss833644380	Aug 21, 2014 (142)
35	EVA-GONL	ss980450173	Aug 21, 2014 (142)
36	JMKIDD_LAB	ss1071787162	Aug 21, 2014 (142)
37	1000GENOMES	ss1310980111	Aug 21, 2014 (142)
38	HAMMER_LAB	ss1397383483	Sep 08, 2015 (146)
39	DDI	ss1429982729	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1580687452	Apr 01, 2015 (144)
41	EVA_DECODE	ss1589954201	Apr 01, 2015 (144)
42	EVA_UK10K_ALSPAC	ss1610736403	Apr 01, 2015 (144)
43	EVA_UK10K_TWINSUK	ss1653730436	Apr 01, 2015 (144)
44	EVA_SVP	ss1712693103	Apr 01, 2015 (144)
45	HAMMER_LAB	ss1801909811	Sep 08, 2015 (146)
46	WEILL_CORNELL_DGM	ss1923690237	Feb 12, 2016 (147)
47	GENOMED	ss1969816836	Jul 19, 2016 (147)
48	JJLAB	ss2022431067	Sep 14, 2016 (149)
49	USC_VALOUEV	ss2150560245	Dec 20, 2016 (150)
50	HUMAN_LONGEVITY	ss2265425779	Dec 20, 2016 (150)
51	ILLUMINA	ss2634154522	Nov 08, 2017 (151)
52	GRF	ss2706037116	Nov 08, 2017 (151)
53	GNOMAD	ss2812855262	Nov 08, 2017 (151)
54	AFFY	ss2985298844	Nov 08, 2017 (151)
55	AFFY	ss2985926699	Nov 08, 2017 (151)
56	SWEGEN	ss2995210586	Nov 08, 2017 (151)
57	BIOINF_KMB_FNS_UNIBA	ss3024990803	Nov 08, 2017 (151)
58	CSHL	ss3345861832	Nov 08, 2017 (151)
59	ILLUMINA	ss3629025514	Oct 12, 2018 (152)
60	ILLUMINA	ss3638501717	Oct 12, 2018 (152)
61	ILLUMINA	ss3639253264	Oct 12, 2018 (152)
62	ILLUMINA	ss3639648031	Oct 12, 2018 (152)
63	ILLUMINA	ss3643451900	Oct 12, 2018 (152)
64	URBANLAB	ss3647802646	Oct 12, 2018 (152)
65	ILLUMINA	ss3654070712	Oct 12, 2018 (152)
66	EGCUT_WGS	ss3663106408	Jul 13, 2019 (153)
67	EVA_DECODE	ss3712656953	Jul 13, 2019 (153)
68	ACPOP	ss3731421848	Jul 13, 2019 (153)
69	EVA	ss3762167148	Jul 13, 2019 (153)
70	PACBIO	ss3784801975	Jul 13, 2019 (153)
71	PACBIO	ss3790246634	Jul 13, 2019 (153)
72	PACBIO	ss3795122038	Jul 13, 2019 (153)
73	KHV_HUMAN_GENOMES	ss3805315572	Jul 13, 2019 (153)
74	EVA	ss3828703569	Apr 26, 2020 (154)
75	EVA	ss3837792866	Apr 26, 2020 (154)
76	EVA	ss3843231259	Apr 26, 2020 (154)
77	HGDP	ss3847758957	Apr 26, 2020 (154)
78	SGDP_PRJ	ss3859610756	Apr 26, 2020 (154)
79	KRGDB	ss3905888286	Apr 26, 2020 (154)
80	EVA	ss3985085345	Apr 26, 2021 (155)
81	EVA	ss4017159538	Apr 26, 2021 (155)
82	TOPMED	ss4624642935	Apr 26, 2021 (155)
83	TOMMO_GENOMICS	ss5167078818	Apr 26, 2021 (155)
84	1000G_HIGH_COVERAGE	ss5260288760	Oct 13, 2022 (156)
85	GENOGRAPHIC	ss5314500096	Oct 13, 2022 (156)
86	EVA	ss5350976784	Oct 13, 2022 (156)
87	HUGCELL_USP	ss5458931169	Oct 13, 2022 (156)
88	EVA	ss5507641508	Oct 13, 2022 (156)
89	1000G_HIGH_COVERAGE	ss5541956783	Oct 13, 2022 (156)
90	SANFORD_IMAGENETICS	ss5635665747	Oct 13, 2022 (156)
91	TOMMO_GENOMICS	ss5701810146	Oct 13, 2022 (156)
92	YY_MCH	ss5805354056	Oct 13, 2022 (156)
93	EVA	ss5844424305	Oct 13, 2022 (156)
94	EVA	ss5854356005	Oct 13, 2022 (156)
95	EVA	ss5864677370	Oct 13, 2022 (156)
96	EVA	ss5964056442	Oct 13, 2022 (156)
97	1000Genomes	NC_000004.11 - 100173968	Oct 12, 2018 (152)
98	1000Genomes_30x	NC_000004.12 - 99252811	Oct 13, 2022 (156)
99	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 100173968	Oct 12, 2018 (152)
100	Genome-wide autozygosity in Daghestan	NC_000004.10 - 100392991	Apr 26, 2020 (154)
101	Genetic variation in the Estonian population	NC_000004.11 - 100173968	Oct 12, 2018 (152)
102	Genographic Project	NC_000004.12 - 99252811	Oct 13, 2022 (156)
103	The Danish reference pan genome	NC_000004.11 - 100173968	Apr 26, 2020 (154)
104	gnomAD - Genomes	NC_000004.12 - 99252811	Apr 26, 2021 (155)
105	Genome of the Netherlands Release 5	NC_000004.11 - 100173968	Apr 26, 2020 (154)
106	HGDP-CEPH-db Supplement 1	NC_000004.10 - 100392991	Apr 26, 2020 (154)
107	HapMap	NC_000004.12 - 99252811	Apr 26, 2020 (154)
108	KOREAN population from KRGDB	NC_000004.11 - 100173968	Apr 26, 2020 (154)
109	Northern Sweden	NC_000004.11 - 100173968	Jul 13, 2019 (153)
110	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 100173968	Apr 26, 2021 (155)
111	Qatari	NC_000004.11 - 100173968	Apr 26, 2020 (154)
112	SGDP_PRJ	NC_000004.11 - 100173968	Apr 26, 2020 (154)
113	Siberian	NC_000004.11 - 100173968	Apr 26, 2020 (154)
114	8.3KJPN	NC_000004.11 - 100173968	Apr 26, 2021 (155)
115	14KJPN	NC_000004.12 - 99252811	Oct 13, 2022 (156)
116	TopMed	NC_000004.12 - 99252811	Apr 26, 2021 (155)
117	UK 10K study - Twins	NC_000004.11 - 100173968	Oct 12, 2018 (152)
118	A Vietnamese Genetic Variation Database	NC_000004.11 - 100173968	Jul 13, 2019 (153)
119	ALFA	NC_000004.12 - 99252811	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)
rs58913424	May 25, 2008 (130)
rs386603332	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3639253264, ss3639648031	NC_000004.9:100531145:T:C	NC_000004.12:99252810:T:C	(self)
358885, 436849, ss108170951, ss117113681, ss162380177, ss277844404, ss293147506, ss825555008, ss1397383483, ss1589954201, ss1712693103, ss3643451900, ss3847758957	NC_000004.10:100392990:T:C	NC_000004.12:99252810:T:C	(self)
22422316, 12472626, 8844656, 6852391, 5513655, 13065680, 4706713, 311272, 5732167, 11627736, 3076599, 25048125, 12472626, 2744376, ss221098764, ss232515111, ss239780123, ss537360807, ss557721165, ss651525721, ss833053552, ss833644380, ss980450173, ss1071787162, ss1310980111, ss1429982729, ss1580687452, ss1610736403, ss1653730436, ss1801909811, ss1923690237, ss1969816836, ss2022431067, ss2150560245, ss2634154522, ss2706037116, ss2812855262, ss2985298844, ss2985926699, ss2995210586, ss3345861832, ss3629025514, ss3638501717, ss3654070712, ss3663106408, ss3731421848, ss3762167148, ss3784801975, ss3790246634, ss3795122038, ss3828703569, ss3837792866, ss3859610756, ss3905888286, ss3985085345, ss4017159538, ss5167078818, ss5350976784, ss5507641508, ss5635665747, ss5844424305, ss5964056442	NC_000004.11:100173967:T:C	NC_000004.12:99252810:T:C	(self)
29482718, 29566, 158835863, 2670271, 35647250, 462020491, 8080066622, ss2265425779, ss3024990803, ss3647802646, ss3712656953, ss3805315572, ss3843231259, ss4624642935, ss5260288760, ss5314500096, ss5458931169, ss5541956783, ss5701810146, ss5805354056, ss5854356005, ss5864677370	NC_000004.12:99252810:T:C	NC_000004.12:99252810:T:C	(self)
ss10107056, ss11617566	NT_016354.15:24668671:T:C	NC_000004.12:99252810:T:C	(self)
ss19594470	NT_016354.16:24668671:T:C	NC_000004.12:99252810:T:C	(self)
ss44582612, ss46543406, ss66622886, ss67467634, ss67822129, ss70870953, ss71459814, ss75451567, ss79224490, ss84497085, ss98986803, ss122562356, ss135207887, ss154366184, ss159542350, ss172143140, ss174026830	NT_016354.19:24721688:T:C	NC_000004.12:99252810:T:C	(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 rs6532814

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
Top▲ Help
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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs6532814