Name: rs11264271
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.

rs11264271

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:154829916 (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>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.162802 (43092/264690, TOPMED)
C=0.140329 (19662/140114, GnomAD)
C=0.13703 (6732/49128, ALFA) (+ 19 more)
T=0.30514 (8622/28256, 14KJPN)
T=0.30555 (5121/16760, 8.3KJPN)
C=0.2642 (1692/6404, 1000G_30x)
C=0.2720 (1362/5008, 1000G)
C=0.1237 (554/4480, Estonian)
C=0.1456 (561/3854, ALSPAC)
C=0.1321 (490/3708, TWINSUK)
T=0.2608 (764/2930, KOREAN)
C=0.3139 (639/2036, HGDP_Stanford)
T=0.2631 (482/1832, Korea1K)
C=0.1179 (183/1552, HapMap)
C=0.137 (137/998, GoNL)
C=0.120 (72/600, NorthernSweden)
T=0.273 (66/242, SGDP_PRJ)
C=0.088 (19/216, Qatari)
T=0.476 (100/210, Vietnamese)
C=0.04 (4/94, Ancient Sardinia)
C=0.15 (6/40, GENOME_DK)
T=0.31 (8/26, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KCNN3 : 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	49222	T=0.86283	C=0.13717	0.749299	0.023648	0.227053	22
European	Sub	38842	T=0.86489	C=0.13511	0.747438	0.017661	0.2349	0
African	Sub	4934	T=0.9459	C=0.0541	0.895825	0.004054	0.100122	1
African Others	Sub	180	T=0.967	C=0.033	0.944444	0.011111	0.044444	5
African American	Sub	4754	T=0.9451	C=0.0549	0.893984	0.003786	0.10223	0
Asian	Sub	438	T=0.301	C=0.699	0.100457	0.497717	0.401826	0
East Asian	Sub	372	T=0.280	C=0.720	0.091398	0.532258	0.376344	0
Other Asian	Sub	66	T=0.42	C=0.58	0.151515	0.30303	0.545455	0
Latin American 1	Sub	514	T=0.864	C=0.136	0.750973	0.023346	0.225681	0
Latin American 2	Sub	836	T=0.652	C=0.348	0.454545	0.150718	0.394737	4
South Asian	Sub	162	T=0.654	C=0.346	0.45679	0.148148	0.395062	1
Other	Sub	3496	T=0.8530	C=0.1470	0.728261	0.022311	0.249428	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=0.837198	C=0.162802
gnomAD - Genomes	Global	Study-wide	140114	T=0.859671	C=0.140329
gnomAD - Genomes	European	Sub	75878	T=0.86335	C=0.13665
gnomAD - Genomes	African	Sub	42016	T=0.94009	C=0.05991
gnomAD - Genomes	American	Sub	13630	T=0.71159	C=0.28841
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.8843	C=0.1157
gnomAD - Genomes	East Asian	Sub	3118	T=0.3255	C=0.6745
gnomAD - Genomes	Other	Sub	2152	T=0.8336	C=0.1664
Allele Frequency Aggregator	Total	Global	49128	T=0.86297	C=0.13703
Allele Frequency Aggregator	European	Sub	38766	T=0.86509	C=0.13491
Allele Frequency Aggregator	African	Sub	4934	T=0.9459	C=0.0541
Allele Frequency Aggregator	Other	Sub	3478	T=0.8528	C=0.1472
Allele Frequency Aggregator	Latin American 2	Sub	836	T=0.652	C=0.348
Allele Frequency Aggregator	Latin American 1	Sub	514	T=0.864	C=0.136
Allele Frequency Aggregator	Asian	Sub	438	T=0.301	C=0.699
Allele Frequency Aggregator	South Asian	Sub	162	T=0.654	C=0.346
14KJPN	JAPANESE	Study-wide	28256	T=0.30514	C=0.69486
8.3KJPN	JAPANESE	Study-wide	16760	T=0.30555	C=0.69445
1000Genomes_30x	Global	Study-wide	6404	T=0.7358	C=0.2642
1000Genomes_30x	African	Sub	1786	T=0.9720	C=0.0280
1000Genomes_30x	Europe	Sub	1266	T=0.8863	C=0.1137
1000Genomes_30x	South Asian	Sub	1202	T=0.7146	C=0.2854
1000Genomes_30x	East Asian	Sub	1170	T=0.3162	C=0.6838
1000Genomes_30x	American	Sub	980	T=0.638	C=0.362
1000Genomes	Global	Study-wide	5008	T=0.7280	C=0.2720
1000Genomes	African	Sub	1322	T=0.9766	C=0.0234
1000Genomes	East Asian	Sub	1008	T=0.3264	C=0.6736
1000Genomes	Europe	Sub	1006	T=0.8817	C=0.1183
1000Genomes	South Asian	Sub	978	T=0.715	C=0.285
1000Genomes	American	Sub	694	T=0.634	C=0.366
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8763	C=0.1237
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8544	C=0.1456
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8679	C=0.1321
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.2608	A=0.0000, C=0.7392, G=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2036	T=0.6861	C=0.3139
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	458	T=0.362	C=0.638
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	400	T=0.735	C=0.265
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	346	T=0.905	C=0.095
HGDP-CEPH-db Supplement 1	Europe	Sub	316	T=0.892	C=0.108
HGDP-CEPH-db Supplement 1	Africa	Sub	238	T=0.987	C=0.013
HGDP-CEPH-db Supplement 1	America	Sub	214	T=0.252	C=0.748
HGDP-CEPH-db Supplement 1	Oceania	Sub	64	T=0.83	C=0.17
Korean Genome Project	KOREAN	Study-wide	1832	T=0.2631	C=0.7369
HapMap	Global	Study-wide	1552	T=0.8821	C=0.1179
HapMap	African	Sub	690	T=0.993	C=0.007
HapMap	American	Sub	598	T=0.839	C=0.161
HapMap	Europe	Sub	176	T=0.915	C=0.085
HapMap	Asian	Sub	88	T=0.24	C=0.76
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.863	C=0.137
Northern Sweden	ACPOP	Study-wide	600	T=0.880	C=0.120
SGDP_PRJ	Global	Study-wide	242	T=0.273	C=0.727
Qatari	Global	Study-wide	216	T=0.912	C=0.088
A Vietnamese Genetic Variation Database	Global	Study-wide	210	T=0.476	C=0.524
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	94	T=0.96	C=0.04
The Danish reference pan genome	Danish	Study-wide	40	T=0.85	C=0.15
Siberian	Global	Study-wide	26	T=0.31	C=0.69

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 1	NC_000001.11:g.154829916T>A
GRCh38.p14 chr 1	NC_000001.11:g.154829916T>C
GRCh38.p14 chr 1	NC_000001.11:g.154829916T>G
GRCh37.p13 chr 1	NC_000001.10:g.154802392T>A
GRCh37.p13 chr 1	NC_000001.10:g.154802392T>C
GRCh37.p13 chr 1	NC_000001.10:g.154802392T>G
KCNN3 RefSeqGene	NG_016807.2:g.45363A>T
KCNN3 RefSeqGene	NG_016807.2:g.45363A>G
KCNN3 RefSeqGene	NG_016807.2:g.45363A>C

Gene: KCNN3, potassium calcium-activated channel subfamily N member 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KCNN3 transcript variant 3	NM_001204087.2:c.934-7732… NM_001204087.2:c.934-7732A>T	N/A	Intron Variant
KCNN3 transcript variant 4	NM_001365837.1:c.-6-7732A… NM_001365837.1:c.-6-7732A>T	N/A	Intron Variant
KCNN3 transcript variant 5	NM_001365838.1:c.-6-7732A… NM_001365838.1:c.-6-7732A>T	N/A	Intron Variant
KCNN3 transcript variant 1	NM_002249.6:c.934-7732A>T	N/A	Intron Variant
KCNN3 transcript variant 2	NM_170782.3:c.19-7732A>T	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=	A	C	G
GRCh38.p14 chr 1	NC_000001.11:g.154829916=	NC_000001.11:g.154829916T>A	NC_000001.11:g.154829916T>C	NC_000001.11:g.154829916T>G
GRCh37.p13 chr 1	NC_000001.10:g.154802392=	NC_000001.10:g.154802392T>A	NC_000001.10:g.154802392T>C	NC_000001.10:g.154802392T>G
KCNN3 RefSeqGene	NG_016807.2:g.45363=	NG_016807.2:g.45363A>T	NG_016807.2:g.45363A>G	NG_016807.2:g.45363A>C
KCNN3 transcript variant 3	NM_001204087.1:c.934-7732=	NM_001204087.1:c.934-7732A>T	NM_001204087.1:c.934-7732A>G	NM_001204087.1:c.934-7732A>C
KCNN3 transcript variant 3	NM_001204087.2:c.934-7732=	NM_001204087.2:c.934-7732A>T	NM_001204087.2:c.934-7732A>G	NM_001204087.2:c.934-7732A>C
KCNN3 transcript variant 4	NM_001365837.1:c.-6-7732=	NM_001365837.1:c.-6-7732A>T	NM_001365837.1:c.-6-7732A>G	NM_001365837.1:c.-6-7732A>C
KCNN3 transcript variant 5	NM_001365838.1:c.-6-7732=	NM_001365838.1:c.-6-7732A>T	NM_001365838.1:c.-6-7732A>G	NM_001365838.1:c.-6-7732A>C
KCNN3 transcript variant 1	NM_002249.5:c.934-7732=	NM_002249.5:c.934-7732A>T	NM_002249.5:c.934-7732A>G	NM_002249.5:c.934-7732A>C
KCNN3 transcript variant 1	NM_002249.6:c.934-7732=	NM_002249.6:c.934-7732A>T	NM_002249.6:c.934-7732A>G	NM_002249.6:c.934-7732A>C
KCNN3 transcript variant 2	NM_170782.2:c.19-7732=	NM_170782.2:c.19-7732A>T	NM_170782.2:c.19-7732A>G	NM_170782.2:c.19-7732A>C
KCNN3 transcript variant 2	NM_170782.3:c.19-7732=	NM_170782.3:c.19-7732A>T	NM_170782.3:c.19-7732A>G	NM_170782.3:c.19-7732A>C
KCNN3 transcript variant X1	XM_005245143.1:c.-6-7732=	XM_005245143.1:c.-6-7732A>T	XM_005245143.1:c.-6-7732A>G	XM_005245143.1:c.-6-7732A>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#.

83 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss16406623	Feb 27, 2004 (120)
2	SC_SNP	ss18085167	Feb 27, 2004 (120)
3	SSAHASNP	ss20456215	Apr 05, 2004 (121)
4	ABI	ss43919359	Mar 15, 2006 (126)
5	ILLUMINA	ss66929976	Nov 30, 2006 (127)
6	ILLUMINA	ss67087340	Nov 30, 2006 (127)
7	ILLUMINA	ss68105705	Dec 12, 2006 (127)
8	PERLEGEN	ss68780628	May 17, 2007 (127)
9	ILLUMINA	ss70527961	May 24, 2008 (130)
10	ILLUMINA	ss71058205	May 17, 2007 (127)
11	ILLUMINA	ss74943036	Dec 06, 2007 (129)
12	KRIBB_YJKIM	ss85097303	Dec 15, 2007 (130)
13	HUMANGENOME_JCVI	ss99251300	Feb 05, 2009 (130)
14	BGI	ss102785783	Dec 01, 2009 (131)
15	ENSEMBL	ss139210137	Dec 01, 2009 (131)
16	GMI	ss155755220	Dec 01, 2009 (131)
17	ILLUMINA	ss159976453	Dec 01, 2009 (131)
18	BCM-HGSC-SUB	ss205357708	Jul 04, 2010 (132)
19	1000GENOMES	ss230732633	Jul 14, 2010 (132)
20	1000GENOMES	ss238380386	Jul 15, 2010 (132)
21	GMI	ss276051909	May 04, 2012 (137)
22	GMI	ss284152994	Apr 25, 2013 (138)
23	PJP	ss290637467	May 09, 2011 (134)
24	ILLUMINA	ss479971577	Sep 08, 2015 (146)
25	TISHKOFF	ss554695404	Apr 25, 2013 (138)
26	SSMP	ss648415093	Apr 25, 2013 (138)
27	EVA-GONL	ss975684261	Aug 21, 2014 (142)
28	JMKIDD_LAB	ss1068270862	Aug 21, 2014 (142)
29	1000GENOMES	ss1292932278	Aug 21, 2014 (142)
30	DDI	ss1425979495	Apr 01, 2015 (144)
31	EVA_GENOME_DK	ss1574393301	Apr 01, 2015 (144)
32	EVA_DECODE	ss1585065839	Apr 01, 2015 (144)
33	EVA_UK10K_ALSPAC	ss1601217737	Apr 01, 2015 (144)
34	EVA_UK10K_TWINSUK	ss1644211770	Apr 01, 2015 (144)
35	EVA_SVP	ss1712371101	Apr 01, 2015 (144)
36	WEILL_CORNELL_DGM	ss1918918326	Feb 12, 2016 (147)
37	GENOMED	ss1966867947	Jul 19, 2016 (147)
38	JJLAB	ss2019974688	Sep 14, 2016 (149)
39	USC_VALOUEV	ss2147999292	Dec 20, 2016 (150)
40	HUMAN_LONGEVITY	ss2166555667	Dec 20, 2016 (150)
41	SYSTEMSBIOZJU	ss2624495351	Nov 08, 2017 (151)
42	ILLUMINA	ss2632576396	Nov 08, 2017 (151)
43	ILLUMINA	ss2635003319	Nov 08, 2017 (151)
44	GRF	ss2697972227	Nov 08, 2017 (151)
45	GNOMAD	ss2761335440	Nov 08, 2017 (151)
46	AFFY	ss2984879393	Nov 08, 2017 (151)
47	AFFY	ss2985525168	Nov 08, 2017 (151)
48	SWEGEN	ss2987754795	Nov 08, 2017 (151)
49	BIOINF_KMB_FNS_UNIBA	ss3023744570	Nov 08, 2017 (151)
50	CSHL	ss3343711391	Nov 08, 2017 (151)
51	ILLUMINA	ss3636029477	Oct 11, 2018 (152)
52	ILLUMINA	ss3638910622	Oct 11, 2018 (152)
53	ILLUMINA	ss3639767391	Oct 11, 2018 (152)
54	ILLUMINA	ss3642796705	Oct 11, 2018 (152)
55	ILLUMINA	ss3643820810	Oct 11, 2018 (152)
56	URBANLAB	ss3646791759	Oct 11, 2018 (152)
57	ILLUMINA	ss3653648586	Oct 11, 2018 (152)
58	EGCUT_WGS	ss3655695190	Jul 12, 2019 (153)
59	EVA_DECODE	ss3687785950	Jul 12, 2019 (153)
60	ACPOP	ss3727487161	Jul 12, 2019 (153)
61	EVA	ss3746810223	Jul 12, 2019 (153)
62	KHV_HUMAN_GENOMES	ss3799811739	Jul 12, 2019 (153)
63	EVA	ss3826425068	Apr 25, 2020 (154)
64	EVA	ss3836607181	Apr 25, 2020 (154)
65	EVA	ss3842016415	Apr 25, 2020 (154)
66	HGDP	ss3847349542	Apr 25, 2020 (154)
67	SGDP_PRJ	ss3850010068	Apr 25, 2020 (154)
68	KRGDB	ss3895217006	Apr 25, 2020 (154)
69	KOGIC	ss3945654972	Apr 25, 2020 (154)
70	EVA	ss3984825600	Apr 25, 2021 (155)
71	TOPMED	ss4468362175	Apr 25, 2021 (155)
72	TOMMO_GENOMICS	ss5146491263	Apr 25, 2021 (155)
73	1000G_HIGH_COVERAGE	ss5244298879	Oct 12, 2022 (156)
74	EVA	ss5322060680	Oct 12, 2022 (156)
75	HUGCELL_USP	ss5444891792	Oct 12, 2022 (156)
76	1000G_HIGH_COVERAGE	ss5517629960	Oct 12, 2022 (156)
77	SANFORD_IMAGENETICS	ss5626594710	Oct 12, 2022 (156)
78	TOMMO_GENOMICS	ss5673689459	Oct 12, 2022 (156)
79	YY_MCH	ss5801261648	Oct 12, 2022 (156)
80	EVA	ss5832667808	Oct 12, 2022 (156)
81	EVA	ss5849109632	Oct 12, 2022 (156)
82	EVA	ss5910252481	Oct 12, 2022 (156)
83	EVA	ss5938388702	Oct 12, 2022 (156)
84	1000Genomes	NC_000001.10 - 154802392	Oct 11, 2018 (152)
85	1000Genomes_30x	NC_000001.11 - 154829916	Oct 12, 2022 (156)
86	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 154802392	Oct 11, 2018 (152)
87	Genetic variation in the Estonian population	NC_000001.10 - 154802392	Oct 11, 2018 (152)
88	The Danish reference pan genome	NC_000001.10 - 154802392	Apr 25, 2020 (154)
89	gnomAD - Genomes	NC_000001.11 - 154829916	Apr 25, 2021 (155)
90	Genome of the Netherlands Release 5	NC_000001.10 - 154802392	Apr 25, 2020 (154)
91	HGDP-CEPH-db Supplement 1	NC_000001.9 - 153069016	Apr 25, 2020 (154)
92	HapMap	NC_000001.11 - 154829916	Apr 25, 2020 (154)
93	KOREAN population from KRGDB	NC_000001.10 - 154802392	Apr 25, 2020 (154)
94	Korean Genome Project	NC_000001.11 - 154829916	Apr 25, 2020 (154)
95	Northern Sweden	NC_000001.10 - 154802392	Jul 12, 2019 (153)
96	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 154802392	Apr 25, 2021 (155)
97	Qatari	NC_000001.10 - 154802392	Apr 25, 2020 (154)
98	SGDP_PRJ	NC_000001.10 - 154802392	Apr 25, 2020 (154)
99	Siberian	NC_000001.10 - 154802392	Apr 25, 2020 (154)
100	8.3KJPN	NC_000001.10 - 154802392	Apr 25, 2021 (155)
101	14KJPN	NC_000001.11 - 154829916	Oct 12, 2022 (156)
102	TopMed	NC_000001.11 - 154829916	Apr 25, 2021 (155)
103	UK 10K study - Twins	NC_000001.10 - 154802392	Oct 11, 2018 (152)
104	A Vietnamese Genetic Variation Database	NC_000001.10 - 154802392	Jul 12, 2019 (153)
105	ALFA	NC_000001.11 - 154829916	Apr 25, 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)
rs58576638	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
2394400, ss3895217006	NC_000001.10:154802391:T:A	NC_000001.11:154829915:T:A	(self)
ss3638910622, ss3639767391, ss3643820810	NC_000001.8:151615464:T:C	NC_000001.11:154829915:T:C	(self)
27434, ss205357708, ss276051909, ss284152994, ss290637467, ss1585065839, ss1712371101, ss2635003319, ss3642796705, ss3847349542	NC_000001.9:153069015:T:C	NC_000001.11:154829915:T:C	(self)
3724571, 2025380, 1433438, 1709351, 879835, 2394400, 772026, 51527, 960256, 2027048, 515646, 4460570, 2025380, 435226, ss230732633, ss238380386, ss479971577, ss554695404, ss648415093, ss975684261, ss1068270862, ss1292932278, ss1425979495, ss1574393301, ss1601217737, ss1644211770, ss1918918326, ss1966867947, ss2019974688, ss2147999292, ss2624495351, ss2632576396, ss2697972227, ss2761335440, ss2984879393, ss2985525168, ss2987754795, ss3343711391, ss3636029477, ss3653648586, ss3655695190, ss3727487161, ss3746810223, ss3826425068, ss3836607181, ss3850010068, ss3895217006, ss3984825600, ss5146491263, ss5322060680, ss5626594710, ss5832667808, ss5938388702	NC_000001.10:154802391:T:C	NC_000001.11:154829915:T:C	(self)
5155895, 27100783, 176846, 2032973, 7526563, 31968510, 5306766900, ss2166555667, ss3023744570, ss3646791759, ss3687785950, ss3799811739, ss3842016415, ss3945654972, ss4468362175, ss5244298879, ss5444891792, ss5517629960, ss5673689459, ss5801261648, ss5849109632, ss5910252481	NC_000001.11:154829915:T:C	NC_000001.11:154829915:T:C	(self)
ss43919359, ss66929976, ss67087340, ss68105705, ss68780628, ss70527961, ss71058205, ss74943036, ss85097303, ss99251300, ss102785783, ss139210137, ss155755220, ss159976453	NT_004487.19:6291033:T:C	NC_000001.11:154829915:T:C	(self)
ss16406623, ss18085167, ss20456215	NT_079484.1:1252223:T:C	NC_000001.11:154829915:T:C	(self)
2394400, ss3895217006	NC_000001.10:154802391:T:G	NC_000001.11:154829915:T:G	(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 rs11264271

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11264271