Name: rs10013214
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.

rs10013214

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:184928835 (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: T=0.426355 (112852/264690, TOPMED)
T=0.423716 (59338/140042, GnomAD)
T=0.41674 (30278/72654, ALFA) (+ 21 more)
T=0.27603 (7800/28258, 14KJPN)
T=0.27584 (4623/16760, 8.3KJPN)
T=0.3901 (2498/6404, 1000G_30x)
T=0.3788 (1897/5008, 1000G)
T=0.4103 (1838/4480, Estonian)
T=0.4297 (1656/3854, ALSPAC)
T=0.4088 (1516/3708, TWINSUK)
T=0.2594 (760/2930, KOREAN)
T=0.3445 (718/2084, HGDP_Stanford)
T=0.3990 (755/1892, HapMap)
T=0.2604 (477/1832, Korea1K)
T=0.3686 (418/1134, Daghestan)
T=0.436 (435/998, GoNL)
T=0.400 (240/600, NorthernSweden)
T=0.233 (112/480, SGDP_PRJ)
T=0.352 (76/216, Qatari)
T=0.236 (51/216, Vietnamese)
T=0.32 (22/68, Ancient Sardinia)
T=0.16 (8/50, Siberian)
T=0.50 (20/40, GENOME_DK)
C=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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	72654	T=0.41674	C=0.58326
European	Sub	57344	T=0.41992	C=0.58008
African	Sub	7158	T=0.4732	C=0.5268
African Others	Sub	252	T=0.460	C=0.540
African American	Sub	6906	T=0.4736	C=0.5264
Asian	Sub	192	T=0.328	C=0.672
East Asian	Sub	150	T=0.367	C=0.633
Other Asian	Sub	42	T=0.19	C=0.81
Latin American 1	Sub	254	T=0.386	C=0.614
Latin American 2	Sub	1232	T=0.3929	C=0.6071
South Asian	Sub	4956	T=0.3188	C=0.6812
Other	Sub	1518	T=0.3860	C=0.6140

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=0.426355	C=0.573645
gnomAD - Genomes	Global	Study-wide	140042	T=0.423716	C=0.576284
gnomAD - Genomes	European	Sub	75870	T=0.40144	C=0.59856
gnomAD - Genomes	African	Sub	41924	T=0.48359	C=0.51641
gnomAD - Genomes	American	Sub	13650	T=0.40095	C=0.59905
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.4085	C=0.5915
gnomAD - Genomes	East Asian	Sub	3124	T=0.2823	C=0.7177
gnomAD - Genomes	Other	Sub	2152	T=0.4159	C=0.5841
Allele Frequency Aggregator	Total	Global	72654	T=0.41674	C=0.58326
Allele Frequency Aggregator	European	Sub	57344	T=0.41992	C=0.58008
Allele Frequency Aggregator	African	Sub	7158	T=0.4732	C=0.5268
Allele Frequency Aggregator	South Asian	Sub	4956	T=0.3188	C=0.6812
Allele Frequency Aggregator	Other	Sub	1518	T=0.3860	C=0.6140
Allele Frequency Aggregator	Latin American 2	Sub	1232	T=0.3929	C=0.6071
Allele Frequency Aggregator	Latin American 1	Sub	254	T=0.386	C=0.614
Allele Frequency Aggregator	Asian	Sub	192	T=0.328	C=0.672
14KJPN	JAPANESE	Study-wide	28258	T=0.27603	C=0.72397
8.3KJPN	JAPANESE	Study-wide	16760	T=0.27584	C=0.72416
1000Genomes_30x	Global	Study-wide	6404	T=0.3901	C=0.6099
1000Genomes_30x	African	Sub	1786	T=0.5129	C=0.4871
1000Genomes_30x	Europe	Sub	1266	T=0.4202	C=0.5798
1000Genomes_30x	South Asian	Sub	1202	T=0.3003	C=0.6997
1000Genomes_30x	East Asian	Sub	1170	T=0.2496	C=0.7504
1000Genomes_30x	American	Sub	980	T=0.405	C=0.595
1000Genomes	Global	Study-wide	5008	T=0.3788	C=0.6212
1000Genomes	African	Sub	1322	T=0.5106	C=0.4894
1000Genomes	East Asian	Sub	1008	T=0.2381	C=0.7619
1000Genomes	Europe	Sub	1006	T=0.4135	C=0.5865
1000Genomes	South Asian	Sub	978	T=0.298	C=0.702
1000Genomes	American	Sub	694	T=0.396	C=0.604
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.4103	C=0.5897
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.4297	C=0.5703
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.4088	C=0.5912
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.2594	A=0.0000, C=0.7406, G=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.3445	C=0.6555
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.253	C=0.747
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.321	C=0.679
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.374	C=0.626
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.466	C=0.534
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.570	C=0.430
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.222	C=0.778
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.00	C=1.00
HapMap	Global	Study-wide	1892	T=0.3990	C=0.6010
HapMap	American	Sub	770	T=0.352	C=0.648
HapMap	African	Sub	692	T=0.532	C=0.468
HapMap	Asian	Sub	254	T=0.232	C=0.768
HapMap	Europe	Sub	176	T=0.324	C=0.676
Korean Genome Project	KOREAN	Study-wide	1832	T=0.2604	C=0.7396
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	T=0.3686	C=0.6314
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	T=0.363	C=0.637
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.396	C=0.604
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.336	C=0.664
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.509	C=0.491
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.29	C=0.71
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.28	C=0.72
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.436	C=0.564
Northern Sweden	ACPOP	Study-wide	600	T=0.400	C=0.600
SGDP_PRJ	Global	Study-wide	480	T=0.233	C=0.767
Qatari	Global	Study-wide	216	T=0.352	C=0.648
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.236	C=0.764
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	68	T=0.32	C=0.68
Siberian	Global	Study-wide	50	T=0.16	C=0.84
The Danish reference pan genome	Danish	Study-wide	40	T=0.50	C=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 4	NC_000004.12:g.184928835T>A
GRCh38.p14 chr 4	NC_000004.12:g.184928835T>C
GRCh38.p14 chr 4	NC_000004.12:g.184928835T>G
GRCh37.p13 chr 4	NC_000004.11:g.185849989T>A
GRCh37.p13 chr 4	NC_000004.11:g.185849989T>C
GRCh37.p13 chr 4	NC_000004.11:g.185849989T>G

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 4	NC_000004.12:g.184928835=	NC_000004.12:g.184928835T>A	NC_000004.12:g.184928835T>C	NC_000004.12:g.184928835T>G
GRCh37.p13 chr 4	NC_000004.11:g.185849989=	NC_000004.11:g.185849989T>A	NC_000004.11:g.185849989T>C	NC_000004.11:g.185849989T>G

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#.

100 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss13859454	Dec 05, 2003 (119)
2	CSHL-HAPMAP	ss17020494	Feb 27, 2004 (120)
3	SSAHASNP	ss22038240	Apr 05, 2004 (123)
4	ABI	ss42249271	Mar 14, 2006 (126)
5	ILLUMINA	ss66864391	Dec 01, 2006 (127)
6	ILLUMINA	ss66934006	Dec 01, 2006 (127)
7	ILLUMINA	ss68075283	Dec 12, 2006 (127)
8	ILLUMINA	ss70459756	May 25, 2008 (130)
9	ILLUMINA	ss70980363	May 17, 2007 (127)
10	ILLUMINA	ss75469295	Dec 07, 2007 (129)
11	KRIBB_YJKIM	ss84889834	Dec 15, 2007 (130)
12	BCMHGSC_JDW	ss92928513	Mar 24, 2008 (129)
13	HUMANGENOME_JCVI	ss98898734	Feb 06, 2009 (130)
14	BGI	ss105895403	Feb 06, 2009 (130)
15	1000GENOMES	ss108683673	Jan 23, 2009 (130)
16	1000GENOMES	ss111191473	Jan 25, 2009 (130)
17	ENSEMBL	ss134799379	Dec 01, 2009 (131)
18	ENSEMBL	ss142667047	Dec 01, 2009 (131)
19	ILLUMINA	ss152541538	Dec 01, 2009 (131)
20	GMI	ss154770446	Dec 01, 2009 (131)
21	ILLUMINA	ss159103611	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss162904570	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss165354324	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss167506601	Jul 04, 2010 (132)
25	ILLUMINA	ss169507974	Jul 04, 2010 (132)
26	BUSHMAN	ss199670357	Jul 04, 2010 (132)
27	BCM-HGSC-SUB	ss206301856	Jul 04, 2010 (132)
28	ILLUMINA	ss209082898	Jul 04, 2010 (132)
29	1000GENOMES	ss221433516	Jul 14, 2010 (132)
30	1000GENOMES	ss232764741	Jul 14, 2010 (132)
31	1000GENOMES	ss239976546	Jul 15, 2010 (132)
32	BL	ss253829001	May 09, 2011 (134)
33	GMI	ss278096925	May 04, 2012 (137)
34	GMI	ss285084723	Apr 25, 2013 (138)
35	PJP	ss293279201	May 09, 2011 (134)
36	ILLUMINA	ss536565385	Sep 08, 2015 (146)
37	TISHKOFF	ss558108507	Apr 25, 2013 (138)
38	SSMP	ss651944787	Apr 25, 2013 (138)
39	ILLUMINA	ss832616407	Jul 13, 2019 (153)
40	EVA-GONL	ss981104218	Aug 21, 2014 (142)
41	JMKIDD_LAB	ss1072284723	Aug 21, 2014 (142)
42	1000GENOMES	ss1313391556	Aug 21, 2014 (142)
43	HAMMER_LAB	ss1397400701	Sep 08, 2015 (146)
44	DDI	ss1430189436	Apr 01, 2015 (144)
45	EVA_GENOME_DK	ss1580951050	Apr 01, 2015 (144)
46	EVA_DECODE	ss1590624733	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1612009231	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1655003264	Apr 01, 2015 (144)
49	EVA_SVP	ss1712733520	Apr 01, 2015 (144)
50	HAMMER_LAB	ss1802776921	Sep 08, 2015 (146)
51	WEILL_CORNELL_DGM	ss1924350664	Feb 12, 2016 (147)
52	GENOMED	ss1969975339	Jul 19, 2016 (147)
53	JJLAB	ss2022770704	Sep 14, 2016 (149)
54	USC_VALOUEV	ss2150904969	Dec 20, 2016 (150)
55	HUMAN_LONGEVITY	ss2270387136	Dec 20, 2016 (150)
56	SYSTEMSBIOZJU	ss2625878599	Nov 08, 2017 (151)
57	ILLUMINA	ss2635139873	Nov 08, 2017 (151)
58	GRF	ss2706413256	Nov 08, 2017 (151)
59	GNOMAD	ss2819721263	Nov 08, 2017 (151)
60	SWEGEN	ss2996201256	Nov 08, 2017 (151)
61	BIOINF_KMB_FNS_UNIBA	ss3025166369	Nov 08, 2017 (151)
62	CSHL	ss3346157582	Nov 08, 2017 (151)
63	ILLUMINA	ss3629146424	Oct 12, 2018 (152)
64	ILLUMINA	ss3638531124	Oct 12, 2018 (152)
65	ILLUMINA	ss3639268034	Oct 12, 2018 (152)
66	ILLUMINA	ss3639931979	Oct 12, 2018 (152)
67	ILLUMINA	ss3643478914	Oct 12, 2018 (152)
68	ILLUMINA	ss3643977775	Oct 12, 2018 (152)
69	URBANLAB	ss3647947595	Oct 12, 2018 (152)
70	EGCUT_WGS	ss3664121913	Jul 13, 2019 (153)
71	EVA_DECODE	ss3713843470	Jul 13, 2019 (153)
72	ACPOP	ss3731964654	Jul 13, 2019 (153)
73	EVA	ss3762897858	Jul 13, 2019 (153)
74	PACBIO	ss3784979213	Jul 13, 2019 (153)
75	PACBIO	ss3790400170	Jul 13, 2019 (153)
76	PACBIO	ss3795275925	Jul 13, 2019 (153)
77	KHV_HUMAN_GENOMES	ss3806066199	Jul 13, 2019 (153)
78	EVA	ss3829020748	Apr 26, 2020 (154)
79	EVA	ss3837966811	Apr 26, 2020 (154)
80	EVA	ss3843409069	Apr 26, 2020 (154)
81	HGDP	ss3847776903	Apr 26, 2020 (154)
82	SGDP_PRJ	ss3860896395	Apr 26, 2020 (154)
83	KRGDB	ss3907281599	Apr 26, 2020 (154)
84	KOGIC	ss3955858302	Apr 26, 2020 (154)
85	EVA	ss3985116775	Apr 26, 2021 (155)
86	EVA	ss4017186377	Apr 26, 2021 (155)
87	TOPMED	ss4645554151	Apr 26, 2021 (155)
88	TOMMO_GENOMICS	ss5169776624	Apr 26, 2021 (155)
89	1000G_HIGH_COVERAGE	ss5262411457	Oct 17, 2022 (156)
90	EVA	ss5354813330	Oct 17, 2022 (156)
91	HUGCELL_USP	ss5460821297	Oct 17, 2022 (156)
92	EVA	ss5507876087	Oct 17, 2022 (156)
93	1000G_HIGH_COVERAGE	ss5545244227	Oct 17, 2022 (156)
94	SANFORD_IMAGENETICS	ss5636908067	Oct 17, 2022 (156)
95	TOMMO_GENOMICS	ss5705254533	Oct 17, 2022 (156)
96	YY_MCH	ss5805891591	Oct 17, 2022 (156)
97	EVA	ss5845268323	Oct 17, 2022 (156)
98	EVA	ss5854620047	Oct 17, 2022 (156)
99	EVA	ss5867081539	Oct 17, 2022 (156)
100	EVA	ss5965325900	Oct 17, 2022 (156)
101	1000Genomes	NC_000004.11 - 185849989	Oct 12, 2018 (152)
102	1000Genomes_30x	NC_000004.12 - 184928835	Oct 17, 2022 (156)
103	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 185849989	Oct 12, 2018 (152)
104	Genome-wide autozygosity in Daghestan	NC_000004.10 - 186086983	Apr 26, 2020 (154)
105	Genetic variation in the Estonian population	NC_000004.11 - 185849989	Oct 12, 2018 (152)
106	The Danish reference pan genome	NC_000004.11 - 185849989	Apr 26, 2020 (154)
107	gnomAD - Genomes	NC_000004.12 - 184928835	Apr 26, 2021 (155)
108	Genome of the Netherlands Release 5	NC_000004.11 - 185849989	Apr 26, 2020 (154)
109	HGDP-CEPH-db Supplement 1	NC_000004.10 - 186086983	Apr 26, 2020 (154)
110	HapMap	NC_000004.12 - 184928835	Apr 26, 2020 (154)
111	KOREAN population from KRGDB	NC_000004.11 - 185849989	Apr 26, 2020 (154)
112	Korean Genome Project	NC_000004.12 - 184928835	Apr 26, 2020 (154)
113	Northern Sweden	NC_000004.11 - 185849989	Jul 13, 2019 (153)
114	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 185849989	Apr 26, 2021 (155)
115	Qatari	NC_000004.11 - 185849989	Apr 26, 2020 (154)
116	SGDP_PRJ	NC_000004.11 - 185849989	Apr 26, 2020 (154)
117	Siberian	NC_000004.11 - 185849989	Apr 26, 2020 (154)
118	8.3KJPN	NC_000004.11 - 185849989	Apr 26, 2021 (155)
119	14KJPN	NC_000004.12 - 184928835	Oct 17, 2022 (156)
120	TopMed	NC_000004.12 - 184928835	Apr 26, 2021 (155)
121	UK 10K study - Twins	NC_000004.11 - 185849989	Oct 12, 2018 (152)
122	A Vietnamese Genetic Variation Database	NC_000004.11 - 185849989	Jul 13, 2019 (153)
123	ALFA	NC_000004.12 - 184928835	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)
rs13101763	Sep 24, 2004 (123)
rs60126964	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
14458993, ss3907281599	NC_000004.11:185849988:T:A	NC_000004.12:184928834:T:A	(self)
ss3639268034, ss3639931979, ss3643977775	NC_000004.9:186225137:T:C	NC_000004.12:184928834:T:C	(self)
375881, 454795, ss92928513, ss108683673, ss111191473, ss162904570, ss165354324, ss167506601, ss199670357, ss206301856, ss253829001, ss278096925, ss285084723, ss293279201, ss1397400701, ss1590624733, ss1712733520, ss2635139873, ss3643478914, ss3847776903	NC_000004.10:186086982:T:C	NC_000004.12:184928834:T:C	(self)
24927959, 13873747, 9860161, 7115989, 6151265, 14458993, 5249519, 342702, 6392594, 12913375, 3421323, 27745931, 13873747, 3073613, ss221433516, ss232764741, ss239976546, ss536565385, ss558108507, ss651944787, ss832616407, ss981104218, ss1072284723, ss1313391556, ss1430189436, ss1580951050, ss1612009231, ss1655003264, ss1802776921, ss1924350664, ss1969975339, ss2022770704, ss2150904969, ss2625878599, ss2706413256, ss2819721263, ss2996201256, ss3346157582, ss3629146424, ss3638531124, ss3664121913, ss3731964654, ss3762897858, ss3784979213, ss3790400170, ss3795275925, ss3829020748, ss3837966811, ss3860896395, ss3907281599, ss3985116775, ss4017186377, ss5169776624, ss5354813330, ss5507876087, ss5636908067, ss5845268323, ss5965325900	NC_000004.11:185849988:T:C	NC_000004.12:184928834:T:C	(self)
32770162, 176365528, 2781795, 12236303, 39091637, 482931707, 9927525413, ss2270387136, ss3025166369, ss3647947595, ss3713843470, ss3806066199, ss3843409069, ss3955858302, ss4645554151, ss5262411457, ss5460821297, ss5545244227, ss5705254533, ss5805891591, ss5854620047, ss5867081539	NC_000004.12:184928834:T:C	NC_000004.12:184928834:T:C	(self)
ss42249271, ss66864391, ss66934006, ss68075283, ss70459756, ss70980363, ss75469295, ss84889834, ss98898734, ss105895403, ss134799379, ss142667047, ss152541538, ss154770446, ss159103611, ss169507974, ss209082898	NT_016354.19:110397709:T:C	NC_000004.12:184928834:T:C	(self)
ss13859454, ss17020494, ss22038240	NT_022792.16:18261509:T:C	NC_000004.12:184928834:T:C	(self)
14458993, ss3907281599	NC_000004.11:185849988:T:G	NC_000004.12:184928834: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 rs10013214

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

rs10013214