Name: rs3741721
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.

rs3741721

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:52315248 (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=0.292021 (77295/264690, TOPMED)
T=0.288794 (40456/140086, GnomAD)
T=0.32481 (11013/33906, ALFA) (+ 18 more)
T=0.33113 (9357/28258, 14KJPN)
T=0.32906 (5515/16760, 8.3KJPN)
T=0.2815 (1803/6404, 1000G_30x)
T=0.2885 (1445/5008, 1000G)
T=0.2714 (1239/4566, GO-ESP)
T=0.3906 (1750/4480, Estonian)
T=0.3282 (1265/3854, ALSPAC)
T=0.3379 (1253/3708, TWINSUK)
T=0.3259 (955/2930, KOREAN)
T=0.2246 (425/1892, HapMap)
T=0.362 (361/998, GoNL)
T=0.333 (205/616, Vietnamese)
T=0.303 (182/600, NorthernSweden)
T=0.303 (162/534, MGP)
T=0.206 (102/496, SGDP_PRJ)
T=0.259 (56/216, Qatari)
T=0.24 (12/50, Siberian)
T=0.47 (19/40, GENOME_DK)

Clinical Significance: Reported in ClinVar
Gene : Consequence: KRT83 : 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	33906	T=0.32481	C=0.67519	0.110364	0.460744	0.428892	5
European	Sub	26470	T=0.35266	C=0.64734	0.123461	0.418134	0.458406	0
African	Sub	4326	T=0.1375	C=0.8625	0.016181	0.7411	0.242718	1
African Others	Sub	158	T=0.108	C=0.892	0.012658	0.797468	0.189873	0
African American	Sub	4168	T=0.1387	C=0.8613	0.016315	0.738964	0.244722	1
Asian	Sub	136	T=0.213	C=0.787	0.044118	0.617647	0.338235	0
East Asian	Sub	108	T=0.259	C=0.741	0.055556	0.537037	0.407407	0
Other Asian	Sub	28	T=0.04	C=0.96	0.0	0.928571	0.071429	0
Latin American 1	Sub	182	T=0.302	C=0.698	0.10989	0.505495	0.384615	0
Latin American 2	Sub	754	T=0.414	C=0.586	0.185676	0.35809	0.456233	1
South Asian	Sub	114	T=0.307	C=0.693	0.105263	0.491228	0.403509	0
Other	Sub	1924	T=0.3389	C=0.6611	0.117464	0.439709	0.442827	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.292021	C=0.707979
gnomAD - Genomes	Global	Study-wide	140086	T=0.288794	C=0.711206
gnomAD - Genomes	European	Sub	75860	T=0.34245	C=0.65755
gnomAD - Genomes	African	Sub	41988	T=0.15083	C=0.84917
gnomAD - Genomes	American	Sub	13646	T=0.37901	C=0.62099
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	T=0.3819	C=0.6181
gnomAD - Genomes	East Asian	Sub	3124	T=0.3191	C=0.6809
gnomAD - Genomes	Other	Sub	2150	T=0.3298	C=0.6702
Allele Frequency Aggregator	Total	Global	33906	T=0.32481	C=0.67519
Allele Frequency Aggregator	European	Sub	26470	T=0.35266	C=0.64734
Allele Frequency Aggregator	African	Sub	4326	T=0.1375	C=0.8625
Allele Frequency Aggregator	Other	Sub	1924	T=0.3389	C=0.6611
Allele Frequency Aggregator	Latin American 2	Sub	754	T=0.414	C=0.586
Allele Frequency Aggregator	Latin American 1	Sub	182	T=0.302	C=0.698
Allele Frequency Aggregator	Asian	Sub	136	T=0.213	C=0.787
Allele Frequency Aggregator	South Asian	Sub	114	T=0.307	C=0.693
14KJPN	JAPANESE	Study-wide	28258	T=0.33113	C=0.66887
8.3KJPN	JAPANESE	Study-wide	16760	T=0.32906	C=0.67094
1000Genomes_30x	Global	Study-wide	6404	T=0.2815	C=0.7185
1000Genomes_30x	African	Sub	1786	T=0.1221	C=0.8779
1000Genomes_30x	Europe	Sub	1266	T=0.3460	C=0.6540
1000Genomes_30x	South Asian	Sub	1202	T=0.3120	C=0.6880
1000Genomes_30x	East Asian	Sub	1170	T=0.3239	C=0.6761
1000Genomes_30x	American	Sub	980	T=0.401	C=0.599
1000Genomes	Global	Study-wide	5008	T=0.2885	C=0.7115
1000Genomes	African	Sub	1322	T=0.1286	C=0.8714
1000Genomes	East Asian	Sub	1008	T=0.3224	C=0.6776
1000Genomes	Europe	Sub	1006	T=0.3559	C=0.6441
1000Genomes	South Asian	Sub	978	T=0.311	C=0.689
1000Genomes	American	Sub	694	T=0.415	C=0.585
GO Exome Sequencing Project	Global	Study-wide	4566	T=0.2714	C=0.7286
GO Exome Sequencing Project	European American	Sub	3182	T=0.3338	C=0.6662
GO Exome Sequencing Project	African American	Sub	1384	T=0.1279	C=0.8721
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.3906	C=0.6094
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.3282	C=0.6718
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.3379	C=0.6621
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.3259	A=0.0000, C=0.6741, G=0.0000
HapMap	Global	Study-wide	1892	T=0.2246	C=0.7754
HapMap	American	Sub	770	T=0.294	C=0.706
HapMap	African	Sub	692	T=0.066	C=0.934
HapMap	Asian	Sub	254	T=0.319	C=0.681
HapMap	Europe	Sub	176	T=0.409	C=0.591
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.362	C=0.638
A Vietnamese Genetic Variation Database	Global	Study-wide	616	T=0.333	C=0.667
Northern Sweden	ACPOP	Study-wide	600	T=0.303	C=0.697
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.303	C=0.697
SGDP_PRJ	Global	Study-wide	496	T=0.206	C=0.794
Qatari	Global	Study-wide	216	T=0.259	C=0.741
Siberian	Global	Study-wide	50	T=0.24	C=0.76
The Danish reference pan genome	Danish	Study-wide	40	T=0.47	C=0.53

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 12	NC_000012.12:g.52315248T>A
GRCh38.p14 chr 12	NC_000012.12:g.52315248T>C
GRCh38.p14 chr 12	NC_000012.12:g.52315248T>G
GRCh37.p13 chr 12	NC_000012.11:g.52709032T>A
GRCh37.p13 chr 12	NC_000012.11:g.52709032T>C
GRCh37.p13 chr 12	NC_000012.11:g.52709032T>G
KRT83 RefSeqGene (LRG_1302)	NG_008352.1:g.11151A>T
KRT83 RefSeqGene (LRG_1302)	NG_008352.1:g.11151A>G
KRT83 RefSeqGene (LRG_1302)	NG_008352.1:g.11151A>C

Gene: KRT83, keratin 83 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KRT83 transcript	NM_002282.3:c.1294+64A>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.

Allele: C (allele ID: 1270570 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001693560.1	not provided	Benign

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 12	NC_000012.12:g.52315248=	NC_000012.12:g.52315248T>A	NC_000012.12:g.52315248T>C	NC_000012.12:g.52315248T>G
GRCh37.p13 chr 12	NC_000012.11:g.52709032=	NC_000012.11:g.52709032T>A	NC_000012.11:g.52709032T>C	NC_000012.11:g.52709032T>G
KRT83 RefSeqGene (LRG_1302)	NG_008352.1:g.11151=	NG_008352.1:g.11151A>T	NG_008352.1:g.11151A>G	NG_008352.1:g.11151A>C
KRT83 transcript	NM_002282.3:c.1294+64=	NM_002282.3:c.1294+64A>T	NM_002282.3:c.1294+64A>G	NM_002282.3:c.1294+64A>C
KRT83 transcript variant X1	XM_005268864.1:c.1282+76=	XM_005268864.1:c.1282+76A>T	XM_005268864.1:c.1282+76A>G	XM_005268864.1:c.1282+76A>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#.

118 SubSNP, 21 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss4927727	Aug 28, 2002 (107)
2	SC_JCM	ss6276310	Feb 20, 2003 (111)
3	WI_SSAHASNP	ss6567952	Feb 20, 2003 (111)
4	BCM_SSAHASNP	ss10715428	Jul 11, 2003 (116)
5	WI_SSAHASNP	ss12183939	Jul 11, 2003 (116)
6	SC_SNP	ss16133368	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss16562864	Feb 27, 2004 (120)
8	CSHL-HAPMAP	ss17450722	Feb 27, 2004 (120)
9	SSAHASNP	ss20902254	Apr 05, 2004 (121)
10	ILLUMINA	ss65751287	Oct 16, 2006 (127)
11	ILLUMINA	ss74982326	Dec 06, 2007 (129)
12	HGSV	ss77434412	Dec 06, 2007 (129)
13	HGSV	ss78921734	Dec 06, 2007 (129)
14	HGSV	ss82719941	Dec 15, 2007 (130)
15	HGSV	ss85236300	Dec 15, 2007 (130)
16	BCMHGSC_JDW	ss89153286	Mar 24, 2008 (129)
17	1000GENOMES	ss111943258	Jan 25, 2009 (130)
18	1000GENOMES	ss113545449	Jan 25, 2009 (130)
19	ILLUMINA-UK	ss118807126	Feb 14, 2009 (130)
20	KRIBB_YJKIM	ss119458499	Dec 01, 2009 (131)
21	ENSEMBL	ss133167755	Dec 01, 2009 (131)
22	ENSEMBL	ss137438120	Dec 01, 2009 (131)
23	GMI	ss157476377	Dec 01, 2009 (131)
24	COMPLETE_GENOMICS	ss168307251	Jul 04, 2010 (132)
25	COMPLETE_GENOMICS	ss169846069	Jul 04, 2010 (132)
26	ILLUMINA	ss173618207	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss175128719	Jul 04, 2010 (132)
28	BUSHMAN	ss198182793	Jul 04, 2010 (132)
29	BCM-HGSC-SUB	ss208140867	Jul 04, 2010 (132)
30	1000GENOMES	ss225754955	Jul 14, 2010 (132)
31	1000GENOMES	ss235936331	Jul 15, 2010 (132)
32	1000GENOMES	ss242495459	Jul 15, 2010 (132)
33	BL	ss255120989	May 09, 2011 (134)
34	GMI	ss281397964	May 04, 2012 (137)
35	GMI	ss286562049	Apr 25, 2013 (138)
36	PJP	ss291251187	May 09, 2011 (134)
37	ILLUMINA	ss479395587	May 04, 2012 (137)
38	ILLUMINA	ss483077723	May 04, 2012 (137)
39	CLINSEQ_SNP	ss491665301	May 04, 2012 (137)
40	ILLUMINA	ss532952209	Sep 08, 2015 (146)
41	TISHKOFF	ss563168392	Apr 25, 2013 (138)
42	SSMP	ss658724076	Apr 25, 2013 (138)
43	NHLBI-ESP	ss713092780	Apr 25, 2013 (138)
44	ILLUMINA	ss779578756	Sep 08, 2015 (146)
45	ILLUMINA	ss780970864	Sep 08, 2015 (146)
46	ILLUMINA	ss835050272	Sep 08, 2015 (146)
47	JMKIDD_LAB	ss974483656	Aug 21, 2014 (142)
48	EVA-GONL	ss989537737	Aug 21, 2014 (142)
49	JMKIDD_LAB	ss1067533978	Aug 21, 2014 (142)
50	JMKIDD_LAB	ss1078463674	Aug 21, 2014 (142)
51	1000GENOMES	ss1345032742	Aug 21, 2014 (142)
52	DDI	ss1426934326	Apr 01, 2015 (144)
53	EVA_GENOME_DK	ss1576285625	Apr 01, 2015 (144)
54	EVA_DECODE	ss1599209269	Apr 01, 2015 (144)
55	EVA_UK10K_ALSPAC	ss1628599668	Apr 01, 2015 (144)
56	EVA_UK10K_TWINSUK	ss1671593701	Apr 01, 2015 (144)
57	EVA_MGP	ss1711330277	Apr 01, 2015 (144)
58	EVA_SVP	ss1713327872	Apr 01, 2015 (144)
59	HAMMER_LAB	ss1807247292	Sep 08, 2015 (146)
60	WEILL_CORNELL_DGM	ss1932902177	Feb 12, 2016 (147)
61	GENOMED	ss1967590619	Jul 19, 2016 (147)
62	JJLAB	ss2027202089	Sep 14, 2016 (149)
63	USC_VALOUEV	ss2155540136	Dec 20, 2016 (150)
64	HUMAN_LONGEVITY	ss2189823767	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2628081757	Nov 08, 2017 (151)
66	ILLUMINA	ss2632959712	Nov 08, 2017 (151)
67	GRF	ss2699883524	Nov 08, 2017 (151)
68	GNOMAD	ss2910552410	Nov 08, 2017 (151)
69	SWEGEN	ss3009695513	Nov 08, 2017 (151)
70	BIOINF_KMB_FNS_UNIBA	ss3027409491	Nov 08, 2017 (151)
71	CSHL	ss3350065872	Nov 08, 2017 (151)
72	ILLUMINA	ss3626878112	Oct 12, 2018 (152)
73	ILLUMINA	ss3630968854	Oct 12, 2018 (152)
74	ILLUMINA	ss3637963255	Oct 12, 2018 (152)
75	ILLUMINA	ss3641789963	Oct 12, 2018 (152)
76	ILLUMINA	ss3642956869	Oct 12, 2018 (152)
77	OMUKHERJEE_ADBS	ss3646442390	Oct 12, 2018 (152)
78	URBANLAB	ss3649838679	Oct 12, 2018 (152)
79	EGCUT_WGS	ss3676967649	Jul 13, 2019 (153)
80	EVA_DECODE	ss3693679380	Jul 13, 2019 (153)
81	ACPOP	ss3739025579	Jul 13, 2019 (153)
82	EVA	ss3750485155	Jul 13, 2019 (153)
83	PACBIO	ss3787227818	Jul 13, 2019 (153)
84	PACBIO	ss3792329268	Jul 13, 2019 (153)
85	PACBIO	ss3797212055	Jul 13, 2019 (153)
86	KHV_HUMAN_GENOMES	ss3815814423	Jul 13, 2019 (153)
87	EVA	ss3824730240	Apr 27, 2020 (154)
88	EVA	ss3825821663	Apr 27, 2020 (154)
89	EVA	ss3833125049	Apr 27, 2020 (154)
90	EVA	ss3840132698	Apr 27, 2020 (154)
91	EVA	ss3845619156	Apr 27, 2020 (154)
92	SGDP_PRJ	ss3878282696	Apr 27, 2020 (154)
93	KRGDB	ss3926915724	Apr 27, 2020 (154)
94	FSA-LAB	ss3984028531	Apr 26, 2021 (155)
95	EVA	ss3986570342	Apr 26, 2021 (155)
96	EVA	ss4017588974	Apr 26, 2021 (155)
97	TOPMED	ss4918443747	Apr 26, 2021 (155)
98	TOMMO_GENOMICS	ss5206342034	Apr 26, 2021 (155)
99	1000G_HIGH_COVERAGE	ss5290824820	Oct 13, 2022 (156)
100	EVA	ss5315621034	Oct 13, 2022 (156)
101	EVA	ss5405663733	Oct 13, 2022 (156)
102	HUGCELL_USP	ss5485576527	Oct 13, 2022 (156)
103	EVA	ss5510705706	Oct 13, 2022 (156)
104	1000G_HIGH_COVERAGE	ss5588318912	Oct 13, 2022 (156)
105	EVA	ss5623957699	Oct 13, 2022 (156)
106	EVA	ss5624032831	Oct 13, 2022 (156)
107	SANFORD_IMAGENETICS	ss5653161943	Oct 13, 2022 (156)
108	TOMMO_GENOMICS	ss5756139837	Oct 13, 2022 (156)
109	EVA	ss5800065033	Oct 13, 2022 (156)
110	EVA	ss5800177361	Oct 13, 2022 (156)
111	YY_MCH	ss5813302190	Oct 13, 2022 (156)
112	EVA	ss5837972057	Oct 13, 2022 (156)
113	EVA	ss5848352781	Oct 13, 2022 (156)
114	EVA	ss5850383011	Oct 13, 2022 (156)
115	EVA	ss5904410465	Oct 13, 2022 (156)
116	EVA	ss5944525167	Oct 13, 2022 (156)
117	EVA	ss5980739747	Oct 13, 2022 (156)
118	EVA	ss5981275799	Oct 13, 2022 (156)
119	1000Genomes	NC_000012.11 - 52709032	Oct 12, 2018 (152)
120	1000Genomes_30x	NC_000012.12 - 52315248	Oct 13, 2022 (156)
121	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 52709032	Oct 12, 2018 (152)
122	Genetic variation in the Estonian population	NC_000012.11 - 52709032	Oct 12, 2018 (152)
123	The Danish reference pan genome	NC_000012.11 - 52709032	Apr 27, 2020 (154)
124	gnomAD - Genomes	NC_000012.12 - 52315248	Apr 26, 2021 (155)
125	GO Exome Sequencing Project	NC_000012.11 - 52709032	Oct 12, 2018 (152)
126	Genome of the Netherlands Release 5	NC_000012.11 - 52709032	Apr 27, 2020 (154)
127	HapMap	NC_000012.12 - 52315248	Apr 27, 2020 (154)
128	KOREAN population from KRGDB	NC_000012.11 - 52709032	Apr 27, 2020 (154)
129	Medical Genome Project healthy controls from Spanish population	NC_000012.11 - 52709032	Apr 27, 2020 (154)
130	Northern Sweden	NC_000012.11 - 52709032	Jul 13, 2019 (153)
131	Qatari	NC_000012.11 - 52709032	Apr 27, 2020 (154)
132	SGDP_PRJ	NC_000012.11 - 52709032	Apr 27, 2020 (154)
133	Siberian	NC_000012.11 - 52709032	Apr 27, 2020 (154)
134	8.3KJPN	NC_000012.11 - 52709032	Apr 26, 2021 (155)
135	14KJPN	NC_000012.12 - 52315248	Oct 13, 2022 (156)
136	TopMed	NC_000012.12 - 52315248	Apr 26, 2021 (155)
137	UK 10K study - Twins	NC_000012.11 - 52709032	Oct 12, 2018 (152)
138	A Vietnamese Genetic Variation Database	NC_000012.11 - 52709032	Jul 13, 2019 (153)
139	ALFA	NC_000012.12 - 52315248	Apr 26, 2021 (155)
140	ClinVar	RCV001693560.1	Oct 13, 2022 (156)

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)
rs60409682	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
34093118, ss3926915724	NC_000012.11:52709031:T:A	NC_000012.12:52315247:T:A	(self)
ss77434412, ss78921734, ss82719941, ss85236300	NC_000012.9:50995298:T:C	NC_000012.12:52315247:T:C	(self)
ss89153286, ss111943258, ss113545449, ss118807126, ss168307251, ss169846069, ss175128719, ss198182793, ss208140867, ss255120989, ss281397964, ss286562049, ss291251187, ss483077723, ss491665301, ss1599209269, ss1713327872, ss3642956869	NC_000012.10:50995298:T:C	NC_000012.12:52315247:T:C	(self)
57782434, 32084933, 22705897, 2965236, 1187718, 14317569, 34093118, 446037, 12310444, 14944107, 30299676, 8056490, 64311341, 32084933, 7122621, ss225754955, ss235936331, ss242495459, ss479395587, ss532952209, ss563168392, ss658724076, ss713092780, ss779578756, ss780970864, ss835050272, ss974483656, ss989537737, ss1067533978, ss1078463674, ss1345032742, ss1426934326, ss1576285625, ss1628599668, ss1671593701, ss1711330277, ss1807247292, ss1932902177, ss1967590619, ss2027202089, ss2155540136, ss2628081757, ss2632959712, ss2699883524, ss2910552410, ss3009695513, ss3350065872, ss3626878112, ss3630968854, ss3637963255, ss3641789963, ss3646442390, ss3676967649, ss3739025579, ss3750485155, ss3787227818, ss3792329268, ss3797212055, ss3824730240, ss3825821663, ss3833125049, ss3840132698, ss3878282696, ss3926915724, ss3984028531, ss3986570342, ss4017588974, ss5206342034, ss5315621034, ss5405663733, ss5510705706, ss5623957699, ss5624032831, ss5653161943, ss5800065033, ss5800177361, ss5837972057, ss5848352781, ss5944525167, ss5980739747, ss5981275799	NC_000012.11:52709031:T:C	NC_000012.12:52315247:T:C	(self)
RCV001693560.1, 75844847, 407467272, 816833, 89976941, 133989404, 3847004111, ss2189823767, ss3027409491, ss3649838679, ss3693679380, ss3815814423, ss3845619156, ss4918443747, ss5290824820, ss5485576527, ss5588318912, ss5756139837, ss5813302190, ss5850383011, ss5904410465	NC_000012.12:52315247:T:C	NC_000012.12:52315247:T:C	(self)
ss10715428, ss12183939, ss16133368, ss16562864, ss17450722, ss20902254	NT_029419.10:14852337:T:C	NC_000012.12:52315247:T:C	(self)
ss4927727, ss6276310, ss6567952, ss65751287, ss74982326, ss119458499, ss133167755, ss137438120, ss157476377, ss173618207	NT_029419.12:14852337:T:C	NC_000012.12:52315247:T:C	(self)
34093118, ss3926915724	NC_000012.11:52709031:T:G	NC_000012.12:52315247: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 rs3741721

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.
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

rs3741721