Name: rs10000543
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.

rs10000543

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:31369166 (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=0.150070 (39722/264690, TOPMED)
T=0.141918 (19885/140116, GnomAD)
T=0.153878 (21205/137804, ALFA) (+ 20 more)
T=0.16102 (12672/78700, PAGE_STUDY)
T=0.21704 (6133/28258, 14KJPN)
T=0.21671 (3632/16760, 8.3KJPN)
T=0.1919 (1229/6404, 1000G_30x)
T=0.1915 (959/5008, 1000G)
T=0.1676 (751/4480, Estonian)
T=0.1565 (603/3854, ALSPAC)
T=0.1427 (529/3708, TWINSUK)
T=0.2440 (715/2930, KOREAN)
T=0.2032 (423/2082, HGDP_Stanford)
T=0.1615 (305/1888, HapMap)
T=0.163 (163/998, GoNL)
T=0.214 (167/780, PRJEB37584)
T=0.165 (99/600, NorthernSweden)
T=0.159 (83/522, SGDP_PRJ)
T=0.157 (34/216, Qatari)
T=0.208 (44/212, Vietnamese)
T=0.11 (6/54, Siberian)
T=0.20 (8/40, GENOME_DK)
T=0.17 (4/24, Ancient Sardinia)

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	137804	T=0.153878	C=0.846122
European	Sub	124026	T=0.151404	C=0.848596
African	Sub	4762	T=0.1023	C=0.8977
African Others	Sub	170	T=0.106	C=0.894
African American	Sub	4592	T=0.1021	C=0.8979
Asian	Sub	222	T=0.212	C=0.788
East Asian	Sub	180	T=0.239	C=0.761
Other Asian	Sub	42	T=0.10	C=0.90
Latin American 1	Sub	262	T=0.164	C=0.836
Latin American 2	Sub	1252	T=0.2372	C=0.7628
South Asian	Sub	4942	T=0.2289	C=0.7711
Other	Sub	2338	T=0.1805	C=0.8195

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=0.150070	C=0.849930
gnomAD - Genomes	Global	Study-wide	140116	T=0.141918	C=0.858082
gnomAD - Genomes	European	Sub	75892	T=0.14932	C=0.85068
gnomAD - Genomes	African	Sub	41980	T=0.10262	C=0.89738
gnomAD - Genomes	American	Sub	13644	T=0.21174	C=0.78826
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.1162	C=0.8838
gnomAD - Genomes	East Asian	Sub	3130	T=0.2035	C=0.7965
gnomAD - Genomes	Other	Sub	2148	T=0.1550	C=0.8450
Allele Frequency Aggregator	Total	Global	137804	T=0.153878	C=0.846122
Allele Frequency Aggregator	European	Sub	124026	T=0.151404	C=0.848596
Allele Frequency Aggregator	South Asian	Sub	4942	T=0.2289	C=0.7711
Allele Frequency Aggregator	African	Sub	4762	T=0.1023	C=0.8977
Allele Frequency Aggregator	Other	Sub	2338	T=0.1805	C=0.8195
Allele Frequency Aggregator	Latin American 2	Sub	1252	T=0.2372	C=0.7628
Allele Frequency Aggregator	Latin American 1	Sub	262	T=0.164	C=0.836
Allele Frequency Aggregator	Asian	Sub	222	T=0.212	C=0.788
The PAGE Study	Global	Study-wide	78700	T=0.16102	C=0.83898
The PAGE Study	AfricanAmerican	Sub	32516	T=0.10635	C=0.89365
The PAGE Study	Mexican	Sub	10810	T=0.26022	C=0.73978
The PAGE Study	Asian	Sub	8318	T=0.2109	C=0.7891
The PAGE Study	PuertoRican	Sub	7918	T=0.1560	C=0.8440
The PAGE Study	NativeHawaiian	Sub	4532	T=0.1593	C=0.8407
The PAGE Study	Cuban	Sub	4230	T=0.1586	C=0.8414
The PAGE Study	Dominican	Sub	3828	T=0.1249	C=0.8751
The PAGE Study	CentralAmerican	Sub	2450	T=0.2588	C=0.7412
The PAGE Study	SouthAmerican	Sub	1982	T=0.2563	C=0.7437
The PAGE Study	NativeAmerican	Sub	1260	T=0.1667	C=0.8333
The PAGE Study	SouthAsian	Sub	856	T=0.221	C=0.779
14KJPN	JAPANESE	Study-wide	28258	T=0.21704	C=0.78296
8.3KJPN	JAPANESE	Study-wide	16760	T=0.21671	C=0.78329
1000Genomes_30x	Global	Study-wide	6404	T=0.1919	C=0.8081
1000Genomes_30x	African	Sub	1786	T=0.1204	C=0.8796
1000Genomes_30x	Europe	Sub	1266	T=0.1659	C=0.8341
1000Genomes_30x	South Asian	Sub	1202	T=0.2155	C=0.7845
1000Genomes_30x	East Asian	Sub	1170	T=0.2368	C=0.7632
1000Genomes_30x	American	Sub	980	T=0.273	C=0.727
1000Genomes	Global	Study-wide	5008	T=0.1915	C=0.8085
1000Genomes	African	Sub	1322	T=0.1210	C=0.8790
1000Genomes	East Asian	Sub	1008	T=0.2341	C=0.7659
1000Genomes	Europe	Sub	1006	T=0.1640	C=0.8360
1000Genomes	South Asian	Sub	978	T=0.215	C=0.785
1000Genomes	American	Sub	694	T=0.271	C=0.729
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.1676	C=0.8324
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.1565	C=0.8435
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.1427	C=0.8573
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.2440	A=0.0000, C=0.7560, G=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	T=0.2032	C=0.7968
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.206	C=0.794
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.234	C=0.766
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.174	C=0.826
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.191	C=0.809
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.136	C=0.864
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.333	C=0.667
HGDP-CEPH-db Supplement 1	Oceania	Sub	70	T=0.03	C=0.97
HapMap	Global	Study-wide	1888	T=0.1615	C=0.8385
HapMap	American	Sub	768	T=0.186	C=0.814
HapMap	African	Sub	690	T=0.097	C=0.903
HapMap	Asian	Sub	254	T=0.244	C=0.756
HapMap	Europe	Sub	176	T=0.188	C=0.812
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.163	C=0.837
CNV burdens in cranial meningiomas	Global	Study-wide	780	T=0.214	C=0.786
CNV burdens in cranial meningiomas	CRM	Sub	780	T=0.214	C=0.786
Northern Sweden	ACPOP	Study-wide	600	T=0.165	C=0.835
SGDP_PRJ	Global	Study-wide	522	T=0.159	C=0.841
Qatari	Global	Study-wide	216	T=0.157	C=0.843
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.208	C=0.792
Siberian	Global	Study-wide	54	T=0.11	C=0.89
The Danish reference pan genome	Danish	Study-wide	40	T=0.20	C=0.80
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	24	T=0.17	C=0.83

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.31369166T>A
GRCh38.p14 chr 4	NC_000004.12:g.31369166T>C
GRCh38.p14 chr 4	NC_000004.12:g.31369166T>G
GRCh37.p13 chr 4	NC_000004.11:g.31370788T>A
GRCh37.p13 chr 4	NC_000004.11:g.31370788T>C
GRCh37.p13 chr 4	NC_000004.11:g.31370788T>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.31369166=	NC_000004.12:g.31369166T>A	NC_000004.12:g.31369166T>C	NC_000004.12:g.31369166T>G
GRCh37.p13 chr 4	NC_000004.11:g.31370788=	NC_000004.11:g.31370788T>A	NC_000004.11:g.31370788T>C	NC_000004.11:g.31370788T>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#.

120 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss13846210	Dec 05, 2003 (119)
2	CSHL-HAPMAP	ss17005086	Feb 27, 2004 (120)
3	SSAHASNP	ss22118156	Apr 05, 2004 (121)
4	PERLEGEN	ss23963746	Sep 20, 2004 (123)
5	ABI	ss44517716	Mar 13, 2006 (126)
6	ILLUMINA	ss66696575	Nov 29, 2006 (127)
7	ILLUMINA	ss66863639	Nov 29, 2006 (127)
8	ILLUMINA	ss66932376	Nov 29, 2006 (127)
9	ILLUMINA	ss70355801	May 16, 2007 (127)
10	ILLUMINA	ss70458988	May 25, 2008 (130)
11	ILLUMINA	ss70979532	May 16, 2007 (127)
12	ILLUMINA	ss75623697	Dec 06, 2007 (129)
13	KRIBB_YJKIM	ss84887455	Dec 15, 2007 (130)
14	BCMHGSC_JDW	ss92522567	Mar 23, 2008 (129)
15	HUMANGENOME_JCVI	ss98946328	Feb 05, 2009 (130)
16	1000GENOMES	ss112020352	Jan 25, 2009 (130)
17	1000GENOMES	ss113010017	Jan 25, 2009 (130)
18	ILLUMINA-UK	ss116933411	Feb 14, 2009 (130)
19	ILLUMINA	ss121251328	Dec 01, 2009 (131)
20	ENSEMBL	ss139521637	Dec 01, 2009 (131)
21	ENSEMBL	ss143240734	Dec 01, 2009 (131)
22	ILLUMINA	ss152537517	Dec 01, 2009 (131)
23	ILLUMINA	ss159102842	Dec 01, 2009 (131)
24	COMPLETE_GENOMICS	ss161986085	Jul 04, 2010 (132)
25	COMPLETE_GENOMICS	ss163282793	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss166384358	Jul 04, 2010 (132)
27	ILLUMINA	ss169203529	Jul 04, 2010 (132)
28	ILLUMINA	ss169484667	Jul 04, 2010 (132)
29	BUSHMAN	ss198285874	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss206266328	Jul 04, 2010 (132)
31	1000GENOMES	ss220832655	Jul 14, 2010 (132)
32	1000GENOMES	ss232324280	Jul 14, 2010 (132)
33	1000GENOMES	ss239632164	Jul 15, 2010 (132)
34	BL	ss253024381	May 09, 2011 (134)
35	GMI	ss277637080	May 04, 2012 (137)
36	GMI	ss284874699	Apr 25, 2013 (138)
37	PJP	ss293316785	May 09, 2011 (134)
38	ILLUMINA	ss479153807	May 04, 2012 (137)
39	ILLUMINA	ss536563809	Sep 08, 2015 (146)
40	TISHKOFF	ss557411253	Apr 25, 2013 (138)
41	SSMP	ss651185811	Apr 25, 2013 (138)
42	ILLUMINA	ss825325532	Apr 01, 2015 (144)
43	ILLUMINA	ss831884941	Sep 08, 2015 (146)
44	ILLUMINA	ss832615638	Jul 13, 2019 (153)
45	EVA-GONL	ss979934874	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1071402945	Aug 21, 2014 (142)
47	1000GENOMES	ss1309059150	Aug 21, 2014 (142)
48	DDI	ss1429825560	Apr 01, 2015 (144)
49	EVA_GENOME_DK	ss1580482730	Apr 01, 2015 (144)
50	EVA_DECODE	ss1589428202	Apr 01, 2015 (144)
51	EVA_UK10K_ALSPAC	ss1609744952	Apr 01, 2015 (144)
52	EVA_UK10K_TWINSUK	ss1652738985	Apr 01, 2015 (144)
53	EVA_SVP	ss1712662532	Apr 01, 2015 (144)
54	ILLUMINA	ss1752519305	Sep 08, 2015 (146)
55	HAMMER_LAB	ss1801211652	Sep 08, 2015 (146)
56	WEILL_CORNELL_DGM	ss1923168587	Feb 12, 2016 (147)
57	ILLUMINA	ss1958671931	Feb 12, 2016 (147)
58	GENOMED	ss1969698128	Jul 19, 2016 (147)
59	JJLAB	ss2022163720	Sep 14, 2016 (149)
60	USC_VALOUEV	ss2150273505	Dec 20, 2016 (150)
61	HUMAN_LONGEVITY	ss2261695246	Dec 20, 2016 (150)
62	SYSTEMSBIOZJU	ss2625583183	Nov 08, 2017 (151)
63	ILLUMINA	ss2634101388	Nov 08, 2017 (151)
64	GRF	ss2705725240	Nov 08, 2017 (151)
65	GNOMAD	ss2807372183	Nov 08, 2017 (151)
66	SWEGEN	ss2994391505	Nov 08, 2017 (151)
67	ILLUMINA	ss3022360436	Nov 08, 2017 (151)
68	BIOINF_KMB_FNS_UNIBA	ss3024851309	Nov 08, 2017 (151)
69	CSHL	ss3345620905	Nov 08, 2017 (151)
70	ILLUMINA	ss3625841093	Oct 12, 2018 (152)
71	ILLUMINA	ss3628934214	Oct 12, 2018 (152)
72	ILLUMINA	ss3633330656	Oct 12, 2018 (152)
73	ILLUMINA	ss3634049488	Oct 12, 2018 (152)
74	ILLUMINA	ss3634946817	Oct 12, 2018 (152)
75	ILLUMINA	ss3635732508	Oct 12, 2018 (152)
76	ILLUMINA	ss3637485022	Oct 12, 2018 (152)
77	ILLUMINA	ss3638479281	Oct 12, 2018 (152)
78	ILLUMINA	ss3639242567	Oct 12, 2018 (152)
79	ILLUMINA	ss3639641908	Oct 12, 2018 (152)
80	ILLUMINA	ss3640654113	Oct 12, 2018 (152)
81	ILLUMINA	ss3643431209	Oct 12, 2018 (152)
82	ILLUMINA	ss3644845847	Oct 12, 2018 (152)
83	URBANLAB	ss3647687052	Oct 12, 2018 (152)
84	ILLUMINA	ss3652844222	Oct 12, 2018 (152)
85	EGCUT_WGS	ss3662309111	Jul 13, 2019 (153)
86	EVA_DECODE	ss3711719125	Jul 13, 2019 (153)
87	ILLUMINA	ss3726121572	Jul 13, 2019 (153)
88	ACPOP	ss3730998812	Jul 13, 2019 (153)
89	ILLUMINA	ss3745247092	Jul 13, 2019 (153)
90	EVA	ss3761595459	Jul 13, 2019 (153)
91	PAGE_CC	ss3771114945	Jul 13, 2019 (153)
92	ILLUMINA	ss3772741770	Jul 13, 2019 (153)
93	PACBIO	ss3784663875	Jul 13, 2019 (153)
94	PACBIO	ss3790128915	Jul 13, 2019 (153)
95	PACBIO	ss3795004058	Jul 13, 2019 (153)
96	KHV_HUMAN_GENOMES	ss3804726780	Jul 13, 2019 (153)
97	EVA	ss3828451973	Apr 26, 2020 (154)
98	EVA	ss3837660456	Apr 26, 2020 (154)
99	EVA	ss3843095253	Apr 26, 2020 (154)
100	HGDP	ss3847746048	Apr 26, 2020 (154)
101	SGDP_PRJ	ss3858553488	Apr 26, 2020 (154)
102	KRGDB	ss3904721971	Apr 26, 2020 (154)
103	EVA	ss3984525926	Apr 26, 2021 (155)
104	EVA	ss3985061654	Apr 26, 2021 (155)
105	EVA	ss4017139439	Apr 26, 2021 (155)
106	TOPMED	ss4608143664	Apr 26, 2021 (155)
107	TOMMO_GENOMICS	ss5164894318	Apr 26, 2021 (155)
108	1000G_HIGH_COVERAGE	ss5258594081	Oct 13, 2022 (156)
109	EVA	ss5314947494	Oct 13, 2022 (156)
110	EVA	ss5347904638	Oct 13, 2022 (156)
111	HUGCELL_USP	ss5457439304	Oct 13, 2022 (156)
112	EVA	ss5507447466	Oct 13, 2022 (156)
113	1000G_HIGH_COVERAGE	ss5539319442	Oct 13, 2022 (156)
114	SANFORD_IMAGENETICS	ss5634668888	Oct 13, 2022 (156)
115	TOMMO_GENOMICS	ss5698732741	Oct 13, 2022 (156)
116	YY_MCH	ss5804899103	Oct 13, 2022 (156)
117	EVA	ss5843765826	Oct 13, 2022 (156)
118	EVA	ss5854148662	Oct 13, 2022 (156)
119	EVA	ss5862777052	Oct 13, 2022 (156)
120	EVA	ss5963056960	Oct 13, 2022 (156)
121	1000Genomes	NC_000004.11 - 31370788	Oct 12, 2018 (152)
122	1000Genomes_30x	NC_000004.12 - 31369166	Oct 13, 2022 (156)
123	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 31370788	Oct 12, 2018 (152)
124	Genetic variation in the Estonian population	NC_000004.11 - 31370788	Oct 12, 2018 (152)
125	The Danish reference pan genome	NC_000004.11 - 31370788	Apr 26, 2020 (154)
126	gnomAD - Genomes	NC_000004.12 - 31369166	Apr 26, 2021 (155)
127	Genome of the Netherlands Release 5	NC_000004.11 - 31370788	Apr 26, 2020 (154)
128	HGDP-CEPH-db Supplement 1	NC_000004.10 - 30979886	Apr 26, 2020 (154)
129	HapMap	NC_000004.12 - 31369166	Apr 26, 2020 (154)
130	KOREAN population from KRGDB	NC_000004.11 - 31370788	Apr 26, 2020 (154)
131	Northern Sweden	NC_000004.11 - 31370788	Jul 13, 2019 (153)
132	The PAGE Study	NC_000004.12 - 31369166	Jul 13, 2019 (153)
133	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 31370788	Apr 26, 2021 (155)
134	CNV burdens in cranial meningiomas	NC_000004.11 - 31370788	Apr 26, 2021 (155)
135	Qatari	NC_000004.11 - 31370788	Apr 26, 2020 (154)
136	SGDP_PRJ	NC_000004.11 - 31370788	Apr 26, 2020 (154)
137	Siberian	NC_000004.11 - 31370788	Apr 26, 2020 (154)
138	8.3KJPN	NC_000004.11 - 31370788	Apr 26, 2021 (155)
139	14KJPN	NC_000004.12 - 31369166	Oct 13, 2022 (156)
140	TopMed	NC_000004.12 - 31369166	Apr 26, 2021 (155)
141	UK 10K study - Twins	NC_000004.11 - 31370788	Oct 12, 2018 (152)
142	A Vietnamese Genetic Variation Database	NC_000004.11 - 31370788	Jul 13, 2019 (153)
143	ALFA	NC_000004.12 - 31369166	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)
rs59037684	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11899365, ss3904721971	NC_000004.11:31370787:T:A	NC_000004.12:31369165:T:A	(self)
ss3639242567, ss3639641908	NC_000004.9:31047056:T:C	NC_000004.12:31369165:T:C	(self)
423940, ss92522567, ss112020352, ss113010017, ss116933411, ss161986085, ss163282793, ss166384358, ss198285874, ss206266328, ss253024381, ss277637080, ss284874699, ss293316785, ss825325532, ss1589428202, ss1712662532, ss3643431209, ss3847746048	NC_000004.10:30979885:T:C	NC_000004.12:31369165:T:C	(self)
20429614, 11384262, 8047359, 6647669, 5012045, 11899365, 4283677, 287581, 75285, 5210517, 10570468, 2789859, 22863625, 11384262, 2493506, ss220832655, ss232324280, ss239632164, ss479153807, ss536563809, ss557411253, ss651185811, ss831884941, ss832615638, ss979934874, ss1071402945, ss1309059150, ss1429825560, ss1580482730, ss1609744952, ss1652738985, ss1752519305, ss1801211652, ss1923168587, ss1958671931, ss1969698128, ss2022163720, ss2150273505, ss2625583183, ss2634101388, ss2705725240, ss2807372183, ss2994391505, ss3022360436, ss3345620905, ss3625841093, ss3628934214, ss3633330656, ss3634049488, ss3634946817, ss3635732508, ss3637485022, ss3638479281, ss3640654113, ss3644845847, ss3652844222, ss3662309111, ss3730998812, ss3745247092, ss3761595459, ss3772741770, ss3784663875, ss3790128915, ss3795004058, ss3828451973, ss3837660456, ss3858553488, ss3904721971, ss3984525926, ss3985061654, ss4017139439, ss5164894318, ss5314947494, ss5347904638, ss5507447466, ss5634668888, ss5843765826, ss5963056960	NC_000004.11:31370787:T:C	NC_000004.12:31369165:T:C	(self)
26845377, 144699639, 2586417, 336414, 32569845, 445521220, 11360281309, ss2261695246, ss3024851309, ss3647687052, ss3711719125, ss3726121572, ss3771114945, ss3804726780, ss3843095253, ss4608143664, ss5258594081, ss5457439304, ss5539319442, ss5698732741, ss5804899103, ss5854148662, ss5862777052	NC_000004.12:31369165:T:C	NC_000004.12:31369165:T:C	(self)
ss13846210, ss17005086, ss22118156	NT_006316.15:22046145:T:C	NC_000004.12:31369165:T:C	(self)
ss23963746, ss44517716, ss66696575, ss66863639, ss66932376, ss70355801, ss70458988, ss70979532, ss75623697, ss84887455, ss98946328, ss121251328, ss139521637, ss143240734, ss152537517, ss159102842, ss169203529, ss169484667	NT_006316.16:22552584:T:C	NC_000004.12:31369165:T:C	(self)
11899365, ss3904721971	NC_000004.11:31370787:T:G	NC_000004.12:31369165: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 rs10000543

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

rs10000543