Name: rs9275582
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.

rs9275582

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:32712293 (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=0.227168 (60129/264690, TOPMED)
T=0.228226 (31921/139866, GnomAD)
T=0.217513 (24408/112214, ALFA) (+ 16 more)
T=0.23870 (18783/78688, PAGE_STUDY)
T=0.23862 (6743/28258, 14KJPN)
T=0.24111 (4041/16760, 8.3KJPN)
T=0.2200 (1409/6404, 1000G_30x)
T=0.2214 (1109/5008, 1000G)
T=0.2020 (905/4480, Estonian)
T=0.2758 (808/2930, KOREAN)
T=0.2159 (450/2084, HGDP_Stanford)
T=0.2105 (397/1886, HapMap)
T=0.217 (217/998, GoNL)
T=0.247 (148/600, NorthernSweden)
T=0.185 (40/216, Qatari)
T=0.126 (27/214, Vietnamese)
C=0.433 (84/194, SGDP_PRJ)
T=0.33 (10/30, Ancient Sardinia)
C=0.42 (10/24, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 1 citation
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	112214	C=0.782487	T=0.217513
European	Sub	97702	C=0.78398	T=0.21602
African	Sub	3988	C=0.8019	T=0.1981
African Others	Sub	152	C=0.763	T=0.237
African American	Sub	3836	C=0.8034	T=0.1966
Asian	Sub	450	C=0.773	T=0.227
East Asian	Sub	382	C=0.767	T=0.233
Other Asian	Sub	68	C=0.81	T=0.19
Latin American 1	Sub	310	C=0.790	T=0.210
Latin American 2	Sub	1470	C=0.6993	T=0.3007
South Asian	Sub	170	C=0.818	T=0.182
Other	Sub	8124	C=0.7696	T=0.2304

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	C=0.772832	T=0.227168
gnomAD - Genomes	Global	Study-wide	139866	C=0.771774	T=0.228226
gnomAD - Genomes	European	Sub	75782	C=0.76717	T=0.23283
gnomAD - Genomes	African	Sub	41866	C=0.80839	T=0.19161
gnomAD - Genomes	American	Sub	13624	C=0.70163	T=0.29837
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.6981	T=0.3019
gnomAD - Genomes	East Asian	Sub	3130	C=0.7802	T=0.2198
gnomAD - Genomes	Other	Sub	2142	C=0.7670	T=0.2330
Allele Frequency Aggregator	Total	Global	112214	C=0.782487	T=0.217513
Allele Frequency Aggregator	European	Sub	97702	C=0.78398	T=0.21602
Allele Frequency Aggregator	Other	Sub	8124	C=0.7696	T=0.2304
Allele Frequency Aggregator	African	Sub	3988	C=0.8019	T=0.1981
Allele Frequency Aggregator	Latin American 2	Sub	1470	C=0.6993	T=0.3007
Allele Frequency Aggregator	Asian	Sub	450	C=0.773	T=0.227
Allele Frequency Aggregator	Latin American 1	Sub	310	C=0.790	T=0.210
Allele Frequency Aggregator	South Asian	Sub	170	C=0.818	T=0.182
The PAGE Study	Global	Study-wide	78688	C=0.76130	T=0.23870
The PAGE Study	AfricanAmerican	Sub	32510	C=0.81037	T=0.18963
The PAGE Study	Mexican	Sub	10810	C=0.65957	T=0.34043
The PAGE Study	Asian	Sub	8318	C=0.7665	T=0.2335
The PAGE Study	PuertoRican	Sub	7912	C=0.7329	T=0.2671
The PAGE Study	NativeHawaiian	Sub	4534	C=0.7880	T=0.2120
The PAGE Study	Cuban	Sub	4230	C=0.7522	T=0.2478
The PAGE Study	Dominican	Sub	3828	C=0.7719	T=0.2281
The PAGE Study	CentralAmerican	Sub	2450	C=0.6245	T=0.3755
The PAGE Study	SouthAmerican	Sub	1980	C=0.6793	T=0.3207
The PAGE Study	NativeAmerican	Sub	1260	C=0.7603	T=0.2397
The PAGE Study	SouthAsian	Sub	856	C=0.832	T=0.168
14KJPN	JAPANESE	Study-wide	28258	C=0.76138	T=0.23862
8.3KJPN	JAPANESE	Study-wide	16760	C=0.75889	T=0.24111
1000Genomes_30x	Global	Study-wide	6404	C=0.7800	T=0.2200
1000Genomes_30x	African	Sub	1786	C=0.7990	T=0.2010
1000Genomes_30x	Europe	Sub	1266	C=0.7575	T=0.2425
1000Genomes_30x	South Asian	Sub	1202	C=0.8336	T=0.1664
1000Genomes_30x	East Asian	Sub	1170	C=0.7838	T=0.2162
1000Genomes_30x	American	Sub	980	C=0.704	T=0.296
1000Genomes	Global	Study-wide	5008	C=0.7786	T=0.2214
1000Genomes	African	Sub	1322	C=0.7920	T=0.2080
1000Genomes	East Asian	Sub	1008	C=0.7837	T=0.2163
1000Genomes	Europe	Sub	1006	C=0.7594	T=0.2406
1000Genomes	South Asian	Sub	978	C=0.833	T=0.167
1000Genomes	American	Sub	694	C=0.696	T=0.304
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.7980	T=0.2020
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.7242	T=0.2758
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.7841	T=0.2159
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.785	T=0.215
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.792	T=0.208
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.837	T=0.163
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.787	T=0.212
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.839	T=0.161
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.542	T=0.458
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=1.00	T=0.00
HapMap	Global	Study-wide	1886	C=0.7895	T=0.2105
HapMap	American	Sub	768	C=0.760	T=0.240
HapMap	African	Sub	688	C=0.807	T=0.193
HapMap	Asian	Sub	254	C=0.772	T=0.228
HapMap	Europe	Sub	176	C=0.875	T=0.125
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.783	T=0.217
Northern Sweden	ACPOP	Study-wide	600	C=0.753	T=0.247
Qatari	Global	Study-wide	216	C=0.815	T=0.185
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.874	T=0.126
SGDP_PRJ	Global	Study-wide	194	C=0.433	T=0.567
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	30	C=0.67	T=0.33
Siberian	Global	Study-wide	24	C=0.42	T=0.58

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.32712293C>T
GRCh37.p13 chr 6	NC_000006.11:g.32680070C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.4125579C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.4125685C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.3906543C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.3912139C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.3956389C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.3961974C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.4112413T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.4111711T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.4131590C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.4137210C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.4011027C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.4016612C>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.32712293=	NC_000006.12:g.32712293C>T
GRCh37.p13 chr 6	NC_000006.11:g.32680070=	NC_000006.11:g.32680070C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.4125579=	NT_113891.3:g.4125579C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.4125685=	NT_113891.2:g.4125685C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.3906543=	NT_167248.2:g.3906543C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.3912139=	NT_167248.1:g.3912139C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.3956389=	NT_167245.2:g.3956389C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.3961974=	NT_167245.1:g.3961974C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.4112413T>C	NT_167249.2:g.4112413=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.4111711T>C	NT_167249.1:g.4111711=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.4131590=	NT_167246.2:g.4131590C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.4137210=	NT_167246.1:g.4137210C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.4011027=	NT_167247.2:g.4011027C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.4016612=	NT_167247.1:g.4016612C>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#.

116 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SI_MHC_SNP	ss12700672	Oct 31, 2003 (118)
2	ABI	ss42824142	Mar 14, 2006 (126)
3	ILLUMINA	ss71595758	May 16, 2007 (127)
4	ILLUMINA	ss74915453	Dec 06, 2007 (129)
5	ILLUMINA	ss79290275	Dec 15, 2007 (130)
6	ILLUMINA	ss98238798	May 25, 2008 (130)
7	HUMANGENOME_JCVI	ss98383893	Feb 05, 2009 (130)
8	1000GENOMES	ss109920591	Feb 13, 2009 (137)
9	ILLUMINA	ss122955419	Dec 01, 2009 (135)
10	ILLUMINA	ss154483020	Dec 01, 2009 (135)
11	ILLUMINA	ss159657249	Dec 01, 2009 (135)
12	ILLUMINA	ss160971026	Dec 01, 2009 (135)
13	COMPLETE_GENOMICS	ss162216694	Jul 04, 2010 (132)
14	ILLUMINA	ss172436928	Jul 04, 2010 (135)
15	ILLUMINA	ss174790565	Jul 04, 2010 (135)
16	BUSHMAN	ss201649457	Jul 04, 2010 (132)
17	BCM-HGSC-SUB	ss207490339	Jul 04, 2010 (132)
18	1000GENOMES	ss211818795	Jul 14, 2010 (137)
19	1000GENOMES	ss222318537	Jul 14, 2010 (137)
20	1000GENOMES	ss233415934	Jul 14, 2010 (137)
21	1000GENOMES	ss240482889	Jul 15, 2010 (137)
22	GMI	ss278741591	May 04, 2012 (137)
23	GMI	ss285380883	Apr 25, 2013 (138)
24	ILLUMINA	ss410956636	Sep 17, 2011 (137)
25	ILLUMINA	ss481849174	May 04, 2012 (137)
26	ILLUMINA	ss481881894	May 04, 2012 (137)
27	ILLUMINA	ss482841750	Sep 08, 2015 (146)
28	ILLUMINA	ss485719014	May 04, 2012 (137)
29	ILLUMINA	ss537579744	Sep 08, 2015 (146)
30	TISHKOFF	ss559120839	Apr 25, 2013 (138)
31	SSMP	ss653052326	Apr 25, 2013 (138)
32	ILLUMINA	ss778633652	Sep 08, 2015 (146)
33	ILLUMINA	ss783305162	Sep 08, 2015 (146)
34	ILLUMINA	ss784257365	Sep 08, 2015 (146)
35	ILLUMINA	ss825620793	Jul 19, 2016 (147)
36	ILLUMINA	ss832566550	Sep 08, 2015 (146)
37	ILLUMINA	ss833168038	Jul 13, 2019 (153)
38	ILLUMINA	ss834091297	Sep 08, 2015 (146)
39	EVA-GONL	ss982786361	Aug 21, 2014 (142)
40	JMKIDD_LAB	ss1073512774	Aug 21, 2014 (142)
41	1000GENOMES	ss1319598162	Aug 21, 2014 (142)
42	EVA_DECODE	ss1592320614	Apr 01, 2015 (144)
43	EVA_SVP	ss1712852523	Apr 01, 2015 (144)
44	ILLUMINA	ss1752631192	Sep 08, 2015 (146)
45	HAMMER_LAB	ss1804367504	Sep 08, 2015 (146)
46	WEILL_CORNELL_DGM	ss1926044133	Feb 12, 2016 (147)
47	ILLUMINA	ss1958895065	Feb 12, 2016 (147)
48	GENOMED	ss1970364258	Jul 19, 2016 (147)
49	JJLAB	ss2023656921	Sep 14, 2016 (149)
50	ILLUMINA	ss2094826279	Dec 20, 2016 (150)
51	ILLUMINA	ss2095180120	Dec 20, 2016 (150)
52	USC_VALOUEV	ss2151832657	Dec 20, 2016 (150)
53	HUMAN_LONGEVITY	ss2282993233	Dec 20, 2016 (150)
54	SYSTEMSBIOZJU	ss2626316263	Nov 08, 2017 (151)
55	ILLUMINA	ss2634433551	Nov 08, 2017 (151)
56	GRF	ss2707427465	Nov 08, 2017 (151)
57	SWEGEN	ss2998841266	Nov 08, 2017 (151)
58	ILLUMINA	ss3022605870	Nov 08, 2017 (151)
59	BIOINF_KMB_FNS_UNIBA	ss3025619588	Nov 08, 2017 (151)
60	ILLUMINA	ss3629511452	Oct 12, 2018 (152)
61	ILLUMINA	ss3632351636	Oct 12, 2018 (152)
62	ILLUMINA	ss3633416704	Oct 12, 2018 (152)
63	ILLUMINA	ss3634139297	Oct 12, 2018 (152)
64	ILLUMINA	ss3635059520	Oct 12, 2018 (152)
65	ILLUMINA	ss3635820247	Oct 12, 2018 (152)
66	ILLUMINA	ss3636781452	Oct 12, 2018 (152)
67	ILLUMINA	ss3637573046	Oct 12, 2018 (152)
68	ILLUMINA	ss3638621835	Oct 12, 2018 (152)
69	ILLUMINA	ss3640766819	Oct 12, 2018 (152)
70	ILLUMINA	ss3643563422	Oct 12, 2018 (152)
71	URBANLAB	ss3648321948	Oct 12, 2018 (152)
72	ILLUMINA	ss3653119748	Oct 12, 2018 (152)
73	EGCUT_WGS	ss3666728856	Jul 13, 2019 (153)
74	EVA_DECODE	ss3716939479	Jul 13, 2019 (153)
75	ILLUMINA	ss3726333723	Jul 13, 2019 (153)
76	ACPOP	ss3733381846	Jul 13, 2019 (153)
77	ILLUMINA	ss3744551958	Jul 13, 2019 (153)
78	ILLUMINA	ss3745359477	Jul 13, 2019 (153)
79	EVA	ss3764846632	Jul 13, 2019 (153)
80	PAGE_CC	ss3771282348	Jul 13, 2019 (153)
81	ILLUMINA	ss3772853151	Jul 13, 2019 (153)
82	PACBIO	ss3785437403	Jul 13, 2019 (153)
83	PACBIO	ss3790794558	Jul 13, 2019 (153)
84	PACBIO	ss3795673134	Jul 13, 2019 (153)
85	KHV_HUMAN_GENOMES	ss3808002842	Jul 13, 2019 (153)
86	EVA	ss3829850644	Apr 26, 2020 (154)
87	EVA	ss3838402871	Apr 26, 2020 (154)
88	EVA	ss3843846833	Apr 26, 2020 (154)
89	HGDP	ss3847829613	Apr 26, 2020 (154)
90	SGDP_PRJ	ss3864302489	Apr 26, 2020 (154)
91	KRGDB	ss3911080487	Apr 26, 2020 (154)
92	EVA	ss3985214590	Apr 26, 2021 (155)
93	EVA	ss4017267854	Apr 26, 2021 (155)
94	VINODS	ss4025195602	Apr 26, 2021 (155)
95	VINODS	ss4025252242	Apr 26, 2021 (155)
96	VINODS	ss4025294502	Apr 26, 2021 (155)
97	TOPMED	ss4698586820	Apr 26, 2021 (155)
98	TOMMO_GENOMICS	ss5176911525	Apr 26, 2021 (155)
99	EVA	ss5237395643	Apr 26, 2021 (155)
100	1000G_HIGH_COVERAGE	ss5267973338	Oct 13, 2022 (156)
101	EVA	ss5315144668	Oct 13, 2022 (156)
102	EVA	ss5364778921	Oct 13, 2022 (156)
103	HUGCELL_USP	ss5465694756	Oct 13, 2022 (156)
104	EVA	ss5508437902	Oct 13, 2022 (156)
105	1000G_HIGH_COVERAGE	ss5553648623	Oct 13, 2022 (156)
106	SANFORD_IMAGENETICS	ss5624625304	Oct 13, 2022 (156)
107	SANFORD_IMAGENETICS	ss5640131110	Oct 13, 2022 (156)
108	TOMMO_GENOMICS	ss5714781785	Oct 13, 2022 (156)
109	EVA	ss5799684637	Oct 13, 2022 (156)
110	YY_MCH	ss5807344245	Oct 13, 2022 (156)
111	EVA	ss5842050481	Oct 13, 2022 (156)
112	EVA	ss5847292206	Oct 13, 2022 (156)
113	EVA	ss5855295988	Oct 13, 2022 (156)
114	EVA	ss5883278335	Oct 13, 2022 (156)
115	EVA	ss5968620304	Oct 13, 2022 (156)
116	EVA	ss5979781942	Oct 13, 2022 (156)
117	1000Genomes	NC_000006.11 - 32680070	Oct 12, 2018 (152)
118	1000Genomes_30x	NC_000006.12 - 32712293	Oct 13, 2022 (156)
119	Genetic variation in the Estonian population	NC_000006.11 - 32680070	Oct 12, 2018 (152)
120	gnomAD - Genomes	NC_000006.12 - 32712293	Apr 26, 2021 (155)
121	Genome of the Netherlands Release 5	NC_000006.11 - 32680070	Apr 26, 2020 (154)
122	HGDP-CEPH-db Supplement 1	NC_000006.10 - 32788048	Apr 26, 2020 (154)
123	HapMap	NC_000006.12 - 32712293	Apr 26, 2020 (154)
124	KOREAN population from KRGDB	NC_000006.11 - 32680070	Apr 26, 2020 (154)
125	Northern Sweden	NC_000006.11 - 32680070	Jul 13, 2019 (153)
126	The PAGE Study	NC_000006.12 - 32712293	Jul 13, 2019 (153)
127	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 32680070	Apr 26, 2021 (155)
128	Qatari	NC_000006.11 - 32680070	Apr 26, 2020 (154)
129	SGDP_PRJ	NC_000006.11 - 32680070	Apr 26, 2020 (154)
130	Siberian	NC_000006.11 - 32680070	Apr 26, 2020 (154)
131	8.3KJPN	NC_000006.11 - 32680070	Apr 26, 2021 (155)
132	14KJPN	NC_000006.12 - 32712293	Oct 13, 2022 (156)
133	TopMed	NC_000006.12 - 32712293	Apr 26, 2021 (155)
134	A Vietnamese Genetic Variation Database	NC_000006.11 - 32680070	Jul 13, 2019 (153)
135	ALFA	NC_000006.12 - 32712293	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)
rs59109578	May 25, 2008 (130)
rs74843632	Sep 17, 2011 (135)
rs116831840	May 04, 2012 (137)
rs117072766	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
507505, ss12700672, ss109920591, ss162216694, ss201649457, ss207490339, ss211818795, ss278741591, ss285380883, ss481849174, ss825620793, ss1592320614, ss1712852523, ss3643563422, ss3847829613	NC_000006.10:32788047:C:T	NC_000006.12:32712292:C:T	(self)
31366948, 12467104, 7780800, 18257881, 6666711, 440517, 8086063, 16319469, 4349011, 34880832, 3880294, ss222318537, ss233415934, ss240482889, ss481881894, ss482841750, ss485719014, ss537579744, ss559120839, ss653052326, ss778633652, ss783305162, ss784257365, ss832566550, ss833168038, ss834091297, ss982786361, ss1073512774, ss1319598162, ss1752631192, ss1804367504, ss1926044133, ss1958895065, ss1970364258, ss2023656921, ss2094826279, ss2095180120, ss2151832657, ss2626316263, ss2634433551, ss2707427465, ss2998841266, ss3022605870, ss3629511452, ss3632351636, ss3633416704, ss3634139297, ss3635059520, ss3635820247, ss3636781452, ss3637573046, ss3638621835, ss3640766819, ss3653119748, ss3666728856, ss3733381846, ss3744551958, ss3745359477, ss3764846632, ss3772853151, ss3785437403, ss3790794558, ss3795673134, ss3829850644, ss3838402871, ss3864302489, ss3911080487, ss3985214590, ss4017267854, ss5176911525, ss5237395643, ss5315144668, ss5364778921, ss5508437902, ss5624625304, ss5640131110, ss5799684637, ss5842050481, ss5847292206, ss5968620304, ss5979781942	NC_000006.11:32680069:C:T	NC_000006.12:32712292:C:T	(self)
41174558, 221434114, 3102865, 503817, 48618889, 535964378, 3934144880, ss2282993233, ss3025619588, ss3648321948, ss3716939479, ss3726333723, ss3771282348, ss3808002842, ss3843846833, ss4698586820, ss5267973338, ss5465694756, ss5553648623, ss5714781785, ss5807344245, ss5855295988, ss5883278335	NC_000006.12:32712292:C:T	NC_000006.12:32712292:C:T	(self)
ss42824142, ss71595758, ss74915453, ss79290275, ss98238798, ss98383893, ss122955419, ss154483020, ss159657249, ss160971026, ss172436928, ss174790565, ss410956636	NT_007592.15:32620069:C:T	NC_000006.12:32712292:C:T	(self)
ss4025195602	NT_113891.3:4125578:C:T	NC_000006.12:32712292:C:T	(self)
ss4025252242	NT_167247.2:4011026:C:T	NC_000006.12:32712292:C:T	(self)
ss4025294502	NT_167249.2:4112412:T:T	NC_000006.12:32712292:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs9275582

PMID	Title	Author	Year	Journal
34403736	Fine mapping of the major histocompatibility complex (MHC) in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suggests involvement of both HLA class I and class II loci.	Hajdarevic R et al.	2021	Brain, behavior, and immunity

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

rs9275582