Name: rs6903433
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.

rs6903433

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:32875198 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.124168 (32866/264690, TOPMED)
T=0.128196 (22018/171752, ALFA)
T=0.121409 (17007/140080, GnomAD) (+ 21 more)
T=0.12982 (10217/78700, PAGE_STUDY)
T=0.15873 (4485/28256, 14KJPN)
T=0.16122 (2702/16760, 8.3KJPN)
T=0.1393 (892/6404, 1000G_30x)
T=0.1390 (696/5008, 1000G)
T=0.0926 (415/4480, Estonian)
T=0.1131 (436/3854, ALSPAC)
T=0.1276 (473/3708, TWINSUK)
T=0.1696 (497/2930, KOREAN)
T=0.1145 (128/1118, Daghestan)
T=0.129 (129/998, GoNL)
T=0.186 (147/790, PRJEB37584)
T=0.143 (86/600, NorthernSweden)
T=0.127 (41/322, HapMap)
T=0.046 (10/216, Qatari)
T=0.093 (20/214, Vietnamese)
C=0.446 (50/112, SGDP_PRJ)
T=0.12 (5/40, GENOME_DK)
T=0.08 (2/26, Ancient Sardinia)
C=0.5 (5/10, Siberian)
T=0.5 (5/10, Siberian)

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	171966	C=0.871800	T=0.128200
European	Sub	149024	C=0.871611	T=0.128389
African	Sub	6484	C=0.8930	T=0.1070
African Others	Sub	252	C=0.893	T=0.107
African American	Sub	6232	C=0.8930	T=0.1070
Asian	Sub	6230	C=0.8453	T=0.1547
East Asian	Sub	4440	C=0.8347	T=0.1653
Other Asian	Sub	1790	C=0.8715	T=0.1285
Latin American 1	Sub	442	C=0.907	T=0.093
Latin American 2	Sub	950	C=0.843	T=0.157
South Asian	Sub	276	C=0.862	T=0.138
Other	Sub	8560	C=0.8800	T=0.1200

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	C=0.875832	T=0.124168
Allele Frequency Aggregator	Total	Global	171752	C=0.871804	T=0.128196
Allele Frequency Aggregator	European	Sub	148846	C=0.871612	T=0.128388
Allele Frequency Aggregator	Other	Sub	8538	C=0.8802	T=0.1198
Allele Frequency Aggregator	African	Sub	6470	C=0.8929	T=0.1071
Allele Frequency Aggregator	Asian	Sub	6230	C=0.8453	T=0.1547
Allele Frequency Aggregator	Latin American 2	Sub	950	C=0.843	T=0.157
Allele Frequency Aggregator	Latin American 1	Sub	442	C=0.907	T=0.093
Allele Frequency Aggregator	South Asian	Sub	276	C=0.862	T=0.138
gnomAD - Genomes	Global	Study-wide	140080	C=0.878591	T=0.121409
gnomAD - Genomes	European	Sub	75862	C=0.87162	T=0.12838
gnomAD - Genomes	African	Sub	41976	C=0.88910	T=0.11090
gnomAD - Genomes	American	Sub	13642	C=0.87905	T=0.12095
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.9149	T=0.0851
gnomAD - Genomes	East Asian	Sub	3126	C=0.8621	T=0.1379
gnomAD - Genomes	Other	Sub	2150	C=0.8842	T=0.1158
The PAGE Study	Global	Study-wide	78700	C=0.87018	T=0.12982
The PAGE Study	AfricanAmerican	Sub	32514	C=0.88940	T=0.11060
The PAGE Study	Mexican	Sub	10810	C=0.83811	T=0.16189
The PAGE Study	Asian	Sub	8318	C=0.8586	T=0.1414
The PAGE Study	PuertoRican	Sub	7918	C=0.8841	T=0.1159
The PAGE Study	NativeHawaiian	Sub	4534	C=0.8205	T=0.1795
The PAGE Study	Cuban	Sub	4230	C=0.8901	T=0.1099
The PAGE Study	Dominican	Sub	3828	C=0.8947	T=0.1053
The PAGE Study	CentralAmerican	Sub	2450	C=0.8645	T=0.1355
The PAGE Study	SouthAmerican	Sub	1982	C=0.8158	T=0.1842
The PAGE Study	NativeAmerican	Sub	1260	C=0.8238	T=0.1762
The PAGE Study	SouthAsian	Sub	856	C=0.794	T=0.206
14KJPN	JAPANESE	Study-wide	28256	C=0.84127	T=0.15873
8.3KJPN	JAPANESE	Study-wide	16760	C=0.83878	T=0.16122
1000Genomes_30x	Global	Study-wide	6404	C=0.8607	T=0.1393
1000Genomes_30x	African	Sub	1786	C=0.8998	T=0.1002
1000Genomes_30x	Europe	Sub	1266	C=0.8562	T=0.1438
1000Genomes_30x	South Asian	Sub	1202	C=0.8103	T=0.1897
1000Genomes_30x	East Asian	Sub	1170	C=0.8812	T=0.1188
1000Genomes_30x	American	Sub	980	C=0.833	T=0.167
1000Genomes	Global	Study-wide	5008	C=0.8610	T=0.1390
1000Genomes	African	Sub	1322	C=0.9002	T=0.0998
1000Genomes	East Asian	Sub	1008	C=0.8869	T=0.1131
1000Genomes	Europe	Sub	1006	C=0.8529	T=0.1471
1000Genomes	South Asian	Sub	978	C=0.812	T=0.188
1000Genomes	American	Sub	694	C=0.830	T=0.170
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9074	T=0.0926
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.8869	T=0.1131
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.8724	T=0.1276
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.8304	T=0.1696
Genome-wide autozygosity in Daghestan	Global	Study-wide	1118	C=0.8855	T=0.1145
Genome-wide autozygosity in Daghestan	Daghestan	Sub	612	C=0.895	T=0.105
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.917	T=0.083
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.852	T=0.148
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.870	T=0.130
Genome-wide autozygosity in Daghestan	South Asian	Sub	96	C=0.82	T=0.18
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.92	T=0.08
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.871	T=0.129
CNV burdens in cranial meningiomas	Global	Study-wide	790	C=0.814	T=0.186
CNV burdens in cranial meningiomas	CRM	Sub	790	C=0.814	T=0.186
Northern Sweden	ACPOP	Study-wide	600	C=0.857	T=0.143
HapMap	Global	Study-wide	322	C=0.873	T=0.127
HapMap	American	Sub	120	C=0.850	T=0.150
HapMap	African	Sub	114	C=0.912	T=0.088
HapMap	Asian	Sub	88	C=0.85	T=0.15
Qatari	Global	Study-wide	216	C=0.954	T=0.046
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.907	T=0.093
SGDP_PRJ	Global	Study-wide	112	C=0.446	T=0.554
The Danish reference pan genome	Danish	Study-wide	40	C=0.88	T=0.12
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	26	C=0.92	T=0.08
Siberian	Global	Study-wide	10	C=0.5	T=0.5

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 6	NC_000006.12:g.32875198C>T
GRCh37.p13 chr 6	NC_000006.11:g.32842975C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.4287397C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.4287503C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.4069484C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.4075080C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.4118725T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.4124310T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.4274445C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.4273743C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.4294549C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.4300169C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.4174259C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.4179844C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.2:g.4180057C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.1:g.4129973C>T

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	C=	T
GRCh38.p14 chr 6	NC_000006.12:g.32875198=	NC_000006.12:g.32875198C>T
GRCh37.p13 chr 6	NC_000006.11:g.32842975=	NC_000006.11:g.32842975C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.4287397=	NT_113891.3:g.4287397C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.4287503=	NT_113891.2:g.4287503C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.4069484=	NT_167248.2:g.4069484C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.4075080=	NT_167248.1:g.4075080C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.4118725T>C	NT_167245.2:g.4118725=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.4124310T>C	NT_167245.1:g.4124310=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.4274445=	NT_167249.2:g.4274445C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.4273743=	NT_167249.1:g.4273743C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.4294549=	NT_167246.2:g.4294549C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.4300169=	NT_167246.1:g.4300169C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.4174259=	NT_167247.2:g.4174259C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.4179844=	NT_167247.1:g.4179844C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.2:g.4180057=	NT_167244.2:g.4180057C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.1:g.4129973=	NT_167244.1:g.4129973C>T

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#.

87 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10276899	Jul 11, 2003 (116)
2	PERLEGEN	ss23718317	Sep 20, 2004 (123)
3	SI_MHC_SNP	ss35526509	May 24, 2005 (126)
4	KRIBB_YJKIM	ss65846625	Nov 29, 2006 (127)
5	ILLUMINA-UK	ss116407248	Dec 01, 2009 (131)
6	1000GENOMES	ss211820440	Jul 14, 2010 (137)
7	1000GENOMES	ss222321050	Jul 14, 2010 (137)
8	1000GENOMES	ss233418509	Jul 14, 2010 (137)
9	1000GENOMES	ss240485033	Jul 15, 2010 (137)
10	BL	ss254219099	May 09, 2011 (137)
11	GMI	ss278743946	May 04, 2012 (137)
12	EXOME_CHIP	ss491383825	May 04, 2012 (137)
13	TISHKOFF	ss559122614	Apr 25, 2013 (138)
14	SSMP	ss653054912	Apr 25, 2013 (138)
15	ILLUMINA	ss780686120	Sep 08, 2015 (146)
16	ILLUMINA	ss783359627	Sep 08, 2015 (146)
17	EVA-GONL	ss982789675	Aug 21, 2014 (142)
18	JMKIDD_LAB	ss1073514680	Aug 21, 2014 (142)
19	1000GENOMES	ss1319604273	Aug 21, 2014 (142)
20	HAMMER_LAB	ss1397452287	Sep 08, 2015 (146)
21	EVA_GENOME_DK	ss1581616914	Apr 01, 2015 (144)
22	EVA_DECODE	ss1592323046	Apr 01, 2015 (144)
23	EVA_UK10K_ALSPAC	ss1615295567	Apr 01, 2015 (144)
24	EVA_UK10K_TWINSUK	ss1658289600	Apr 01, 2015 (144)
25	ILLUMINA	ss1752631754	Sep 08, 2015 (146)
26	HAMMER_LAB	ss1804369354	Sep 08, 2015 (146)
27	ILLUMINA	ss1917803744	Feb 12, 2016 (147)
28	WEILL_CORNELL_DGM	ss1926047533	Feb 12, 2016 (147)
29	ILLUMINA	ss1946175072	Feb 12, 2016 (147)
30	ILLUMINA	ss1958896549	Feb 12, 2016 (147)
31	JJLAB	ss2023659626	Sep 14, 2016 (149)
32	ILLUMINA	ss2094826714	Dec 20, 2016 (150)
33	ILLUMINA	ss2095180704	Dec 20, 2016 (150)
34	USC_VALOUEV	ss2151835629	Dec 20, 2016 (150)
35	HUMAN_LONGEVITY	ss2283002232	Dec 20, 2016 (150)
36	SYSTEMSBIOZJU	ss2626317916	Nov 08, 2017 (151)
37	GRF	ss2707430499	Nov 08, 2017 (151)
38	AFFY	ss2985364137	Nov 08, 2017 (151)
39	AFFY	ss2985996622	Nov 08, 2017 (151)
40	SWEGEN	ss2998846195	Nov 08, 2017 (151)
41	ILLUMINA	ss3022607371	Nov 08, 2017 (151)
42	BIOINF_KMB_FNS_UNIBA	ss3025621461	Nov 08, 2017 (151)
43	ILLUMINA	ss3629513640	Oct 12, 2018 (152)
44	ILLUMINA	ss3635060083	Oct 12, 2018 (152)
45	ILLUMINA	ss3640767382	Oct 12, 2018 (152)
46	ILLUMINA	ss3644908111	Oct 12, 2018 (152)
47	ILLUMINA	ss3653121575	Oct 12, 2018 (152)
48	ILLUMINA	ss3653121576	Oct 12, 2018 (152)
49	ILLUMINA	ss3654129885	Oct 12, 2018 (152)
50	EGCUT_WGS	ss3666733131	Jul 13, 2019 (153)
51	EVA_DECODE	ss3716944084	Jul 13, 2019 (153)
52	ILLUMINA	ss3726334872	Jul 13, 2019 (153)
53	ACPOP	ss3733385043	Jul 13, 2019 (153)
54	ILLUMINA	ss3744552201	Jul 13, 2019 (153)
55	ILLUMINA	ss3745360032	Jul 13, 2019 (153)
56	EVA	ss3764850193	Jul 13, 2019 (153)
57	PAGE_CC	ss3771283454	Jul 13, 2019 (153)
58	ILLUMINA	ss3772853700	Jul 13, 2019 (153)
59	KHV_HUMAN_GENOMES	ss3808006537	Jul 13, 2019 (153)
60	EVA	ss3829853443	Apr 26, 2020 (154)
61	EVA	ss3838404709	Apr 26, 2020 (154)
62	EVA	ss3843848750	Apr 26, 2020 (154)
63	SGDP_PRJ	ss3864307623	Apr 26, 2020 (154)
64	KRGDB	ss3911085662	Apr 26, 2020 (154)
65	EVA	ss3984566707	Apr 26, 2021 (155)
66	EVA	ss3985214983	Apr 26, 2021 (155)
67	VINODS	ss4025196532	Apr 26, 2021 (155)
68	VINODS	ss4025236883	Apr 26, 2021 (155)
69	TOPMED	ss4698619598	Apr 26, 2021 (155)
70	TOMMO_GENOMICS	ss5176918974	Apr 26, 2021 (155)
71	EVA	ss5237395848	Apr 26, 2021 (155)
72	1000G_HIGH_COVERAGE	ss5267979677	Oct 13, 2022 (156)
73	EVA	ss5315145541	Oct 13, 2022 (156)
74	EVA	ss5364787423	Oct 13, 2022 (156)
75	HUGCELL_USP	ss5465699698	Oct 13, 2022 (156)
76	EVA	ss5508440594	Oct 13, 2022 (156)
77	1000G_HIGH_COVERAGE	ss5553656422	Oct 13, 2022 (156)
78	SANFORD_IMAGENETICS	ss5624625709	Oct 13, 2022 (156)
79	SANFORD_IMAGENETICS	ss5640136174	Oct 13, 2022 (156)
80	TOMMO_GENOMICS	ss5714791352	Oct 13, 2022 (156)
81	YY_MCH	ss5807348381	Oct 13, 2022 (156)
82	EVA	ss5842054383	Oct 13, 2022 (156)
83	EVA	ss5847292563	Oct 13, 2022 (156)
84	EVA	ss5855298360	Oct 13, 2022 (156)
85	EVA	ss5883284618	Oct 13, 2022 (156)
86	EVA	ss5968624586	Oct 13, 2022 (156)
87	EVA	ss5979782388	Oct 13, 2022 (156)
88	1000Genomes	NC_000006.11 - 32842975	Oct 12, 2018 (152)
89	1000Genomes_30x	NC_000006.12 - 32875198	Oct 13, 2022 (156)
90	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 32842975	Oct 12, 2018 (152)
91	Genome-wide autozygosity in Daghestan	NC_000006.10 - 32950953	Apr 26, 2020 (154)
92	Genetic variation in the Estonian population	NC_000006.11 - 32842975	Oct 12, 2018 (152)
93	The Danish reference pan genome	NC_000006.11 - 32842975	Apr 26, 2020 (154)
94	gnomAD - Genomes	NC_000006.12 - 32875198	Apr 26, 2021 (155)
95	Genome of the Netherlands Release 5	NC_000006.11 - 32842975	Apr 26, 2020 (154)
96	HapMap	NC_000006.12 - 32875198	Apr 26, 2020 (154)
97	KOREAN population from KRGDB	NC_000006.11 - 32842975	Apr 26, 2020 (154)
98	Northern Sweden	NC_000006.11 - 32842975	Jul 13, 2019 (153)
99	The PAGE Study	NC_000006.12 - 32875198	Jul 13, 2019 (153)
100	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 32842975	Apr 26, 2021 (155)
101	CNV burdens in cranial meningiomas	NC_000006.11 - 32842975	Apr 26, 2021 (155)
102	Qatari	NC_000006.11 - 32842975	Apr 26, 2020 (154)
103	SGDP_PRJ	NC_000006.11 - 32842975	Apr 26, 2020 (154)
104	Siberian	NC_000006.11 - 32842975	Apr 26, 2020 (154)
105	8.3KJPN	NC_000006.11 - 32842975	Apr 26, 2021 (155)
106	14KJPN	NC_000006.12 - 32875198	Oct 13, 2022 (156)
107	TopMed	NC_000006.12 - 32875198	Apr 26, 2021 (155)
108	UK 10K study - Twins	NC_000006.11 - 32842975	Oct 12, 2018 (152)
109	A Vietnamese Genetic Variation Database	NC_000006.11 - 32842975	Jul 13, 2019 (153)
110	ALFA	NC_000006.12 - 32875198	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)
rs17430920	Oct 08, 2004 (123)
rs28892575	Mar 10, 2006 (126)
rs115657598	May 04, 2012 (137)
rs117023497	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
426934, ss116407248, ss211820440, ss254219099, ss278743946, ss1397452287, ss1592323046	NC_000006.10:32950952:C:T	NC_000006.12:32875197:C:T	(self)
31373354, 17487489, 12471379, 7781853, 7784005, 18263056, 6669908, 440910, 116113, 8089463, 16324603, 4351983, 34888281, 17487489, 3881994, ss222321050, ss233418509, ss240485033, ss491383825, ss559122614, ss653054912, ss780686120, ss783359627, ss982789675, ss1073514680, ss1319604273, ss1581616914, ss1615295567, ss1658289600, ss1752631754, ss1804369354, ss1917803744, ss1926047533, ss1946175072, ss1958896549, ss2023659626, ss2094826714, ss2095180704, ss2151835629, ss2626317916, ss2707430499, ss2985364137, ss2985996622, ss2998846195, ss3022607371, ss3629513640, ss3635060083, ss3640767382, ss3644908111, ss3653121575, ss3653121576, ss3654129885, ss3666733131, ss3733385043, ss3744552201, ss3745360032, ss3764850193, ss3772853700, ss3829853443, ss3838404709, ss3864307623, ss3911085662, ss3984566707, ss3985214983, ss5176918974, ss5237395848, ss5315145541, ss5364787423, ss5508440594, ss5624625709, ss5640136174, ss5842054383, ss5847292563, ss5968624586, ss5979782388	NC_000006.11:32842974:C:T	NC_000006.12:32875197:C:T	(self)
41182357, 221464352, 3103851, 504923, 48628456, 535997156, 2357971097, ss2283002232, ss3025621461, ss3716944084, ss3726334872, ss3771283454, ss3808006537, ss3843848750, ss4698619598, ss5267979677, ss5465699698, ss5553656422, ss5714791352, ss5807348381, ss5855298360, ss5883284618	NC_000006.12:32875197:C:T	NC_000006.12:32875197:C:T	(self)
ss10276899	NT_007592.13:23640205:C:T	NC_000006.12:32875197:C:T	(self)
ss23718317, ss35526509, ss65846625	NT_007592.15:32782974:C:T	NC_000006.12:32875197:C:T	(self)
ss4025196532	NT_113891.3:4287396:C:T	NC_000006.12:32875197:C:T	(self)
ss4025236883	NT_167246.2:4294548:C:T	NC_000006.12:32875197:C:T	(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 rs6903433

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

rs6903433