Name: rs7732567
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.

rs7732567

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:135604013 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.495614 (131184/264690, TOPMED)
C=0.460068 (92908/201944, ALFA)
T=0.484761 (67882/140032, GnomAD) (+ 20 more)
C=0.38591 (10905/28258, 14KJPN)
C=0.38300 (6419/16760, 8.3KJPN)
T=0.4905 (3141/6404, 1000G_30x)
T=0.4902 (2455/5008, 1000G)
T=0.4795 (2148/4480, Estonian)
C=0.4424 (1705/3854, ALSPAC)
C=0.4258 (1579/3708, TWINSUK)
C=0.3751 (1099/2930, KOREAN)
C=0.4726 (985/2084, HGDP_Stanford)
T=0.4466 (845/1892, HapMap)
C=0.3706 (679/1832, Korea1K)
C=0.4441 (501/1128, Daghestan)
C=0.477 (476/998, GoNL)
C=0.443 (266/600, NorthernSweden)
T=0.337 (134/398, SGDP_PRJ)
T=0.463 (100/216, Qatari)
C=0.443 (94/212, Vietnamese)
C=0.31 (22/72, Ancient Sardinia)
C=0.42 (17/40, GENOME_DK)
T=0.39 (15/38, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC25A48 : 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	201944	T=0.539932	A=0.000000, C=0.460068
European	Sub	175108	T=0.543071	A=0.000000, C=0.456929
African	Sub	6634	T=0.3304	A=0.0000, C=0.6696
African Others	Sub	240	T=0.279	A=0.000, C=0.721
African American	Sub	6394	T=0.3323	A=0.0000, C=0.6677
Asian	Sub	702	T=0.548	A=0.000, C=0.452
East Asian	Sub	556	T=0.567	A=0.000, C=0.433
Other Asian	Sub	146	T=0.479	A=0.000, C=0.521
Latin American 1	Sub	844	T=0.495	A=0.000, C=0.505
Latin American 2	Sub	6908	T=0.6946	A=0.0000, C=0.3054
South Asian	Sub	5042	T=0.5087	A=0.0000, C=0.4913
Other	Sub	6706	T=0.5341	A=0.0000, C=0.4659

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=0.495614	C=0.504386
Allele Frequency Aggregator	Total	Global	201944	T=0.539932	A=0.000000, C=0.460068
Allele Frequency Aggregator	European	Sub	175108	T=0.543071	A=0.000000, C=0.456929
Allele Frequency Aggregator	Latin American 2	Sub	6908	T=0.6946	A=0.0000, C=0.3054
Allele Frequency Aggregator	Other	Sub	6706	T=0.5341	A=0.0000, C=0.4659
Allele Frequency Aggregator	African	Sub	6634	T=0.3304	A=0.0000, C=0.6696
Allele Frequency Aggregator	South Asian	Sub	5042	T=0.5087	A=0.0000, C=0.4913
Allele Frequency Aggregator	Latin American 1	Sub	844	T=0.495	A=0.000, C=0.505
Allele Frequency Aggregator	Asian	Sub	702	T=0.548	A=0.000, C=0.452
gnomAD - Genomes	Global	Study-wide	140032	T=0.484761	C=0.515239
gnomAD - Genomes	European	Sub	75848	T=0.53635	C=0.46365
gnomAD - Genomes	African	Sub	41954	T=0.33451	C=0.66549
gnomAD - Genomes	American	Sub	13640	T=0.63101	C=0.36899
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.4831	C=0.5169
gnomAD - Genomes	East Asian	Sub	3124	T=0.5851	C=0.4149
gnomAD - Genomes	Other	Sub	2144	T=0.5257	C=0.4743
14KJPN	JAPANESE	Study-wide	28258	T=0.61409	C=0.38591
8.3KJPN	JAPANESE	Study-wide	16760	T=0.61700	C=0.38300
1000Genomes_30x	Global	Study-wide	6404	T=0.4905	C=0.5095
1000Genomes_30x	African	Sub	1786	T=0.2973	C=0.7027
1000Genomes_30x	Europe	Sub	1266	T=0.5442	C=0.4558
1000Genomes_30x	South Asian	Sub	1202	T=0.5241	C=0.4759
1000Genomes_30x	East Asian	Sub	1170	T=0.5496	C=0.4504
1000Genomes_30x	American	Sub	980	T=0.661	C=0.339
1000Genomes	Global	Study-wide	5008	T=0.4902	C=0.5098
1000Genomes	African	Sub	1322	T=0.2905	C=0.7095
1000Genomes	East Asian	Sub	1008	T=0.5446	C=0.4554
1000Genomes	Europe	Sub	1006	T=0.5467	C=0.4533
1000Genomes	South Asian	Sub	978	T=0.529	C=0.471
1000Genomes	American	Sub	694	T=0.656	C=0.344
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.4795	C=0.5205
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.5576	C=0.4424
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5742	C=0.4258
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.6249	A=0.0000, C=0.3751
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.5274	C=0.4726
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.623	C=0.377
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.500	C=0.500
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.457	C=0.543
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.572	C=0.428
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.182	C=0.818
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.787	C=0.213
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.58	C=0.42
HapMap	Global	Study-wide	1892	T=0.4466	C=0.5534
HapMap	American	Sub	770	T=0.548	C=0.452
HapMap	African	Sub	692	T=0.282	C=0.718
HapMap	Asian	Sub	254	T=0.563	C=0.437
HapMap	Europe	Sub	176	T=0.483	C=0.517
Korean Genome Project	KOREAN	Study-wide	1832	T=0.6294	C=0.3706
Genome-wide autozygosity in Daghestan	Global	Study-wide	1128	T=0.5559	C=0.4441
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	T=0.575	C=0.425
Genome-wide autozygosity in Daghestan	Near_East	Sub	142	T=0.486	C=0.514
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.615	C=0.385
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.519	C=0.481
Genome-wide autozygosity in Daghestan	South Asian	Sub	94	T=0.48	C=0.52
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.61	C=0.39
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.523	C=0.477
Northern Sweden	ACPOP	Study-wide	600	T=0.557	C=0.443
SGDP_PRJ	Global	Study-wide	398	T=0.337	C=0.663
Qatari	Global	Study-wide	216	T=0.463	C=0.537
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.557	C=0.443
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	72	T=0.69	C=0.31
The Danish reference pan genome	Danish	Study-wide	40	T=0.57	C=0.42
Siberian	Global	Study-wide	38	T=0.39	C=0.61

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 5	NC_000005.10:g.135604013T>A
GRCh38.p14 chr 5	NC_000005.10:g.135604013T>C
GRCh37.p13 chr 5	NC_000005.9:g.134939703T>A
GRCh37.p13 chr 5	NC_000005.9:g.134939703T>C

Gene: SLC25A48, solute carrier family 25 member 48 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC25A48 transcript variant 3	NM_001349335.2:c.-849+244… NM_001349335.2:c.-849+24416T>A	N/A	Intron Variant
SLC25A48 transcript variant 5	NM_001349345.2:c.-849+244… NM_001349345.2:c.-849+24416T>A	N/A	Intron Variant
SLC25A48 transcript variant 1	NM_001349336.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant 2	NM_145282.5:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant 4	NR_146141.2:n.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X9	XM_005271903.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X2	XM_006714544.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X7	XM_006714550.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X14	XM_006714552.3:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X8	XM_011543196.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X10	XM_011543199.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X3	XM_017009087.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X4	XM_017009088.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X6	XM_017009089.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X11	XM_017009091.2:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X1	XM_047416804.1:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X5	XM_047416805.1:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X12	XM_047416806.1:c.	N/A	Genic Upstream Transcript Variant
SLC25A48 transcript variant X13	XM_047416807.1:c.	N/A	Genic Upstream Transcript 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.

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
GRCh38.p14 chr 5	NC_000005.10:g.135604013=	NC_000005.10:g.135604013T>A	NC_000005.10:g.135604013T>C
GRCh37.p13 chr 5	NC_000005.9:g.134939703=	NC_000005.9:g.134939703T>A	NC_000005.9:g.134939703T>C
SLC25A48 transcript variant 3	NM_001349335.2:c.-849+24416=	NM_001349335.2:c.-849+24416T>A	NM_001349335.2:c.-849+24416T>C
SLC25A48 transcript variant 5	NM_001349345.2:c.-849+24416=	NM_001349345.2:c.-849+24416T>A	NM_001349345.2:c.-849+24416T>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#.

123 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11758688	Jul 11, 2003 (116)
2	ABI	ss42640441	Mar 14, 2006 (126)
3	ILLUMINA	ss66788174	Nov 30, 2006 (127)
4	ILLUMINA	ss67823812	Nov 30, 2006 (127)
5	ILLUMINA	ss67986887	Nov 30, 2006 (127)
6	ILLUMINA	ss70946379	May 27, 2008 (130)
7	ILLUMINA	ss71551408	May 17, 2007 (127)
8	ILLUMINA	ss75766849	Dec 06, 2007 (129)
9	ILLUMINA	ss79268075	Dec 16, 2007 (130)
10	KRIBB_YJKIM	ss84715054	Dec 16, 2007 (130)
11	BCMHGSC_JDW	ss93259854	Mar 24, 2008 (129)
12	HUMANGENOME_JCVI	ss98767261	Feb 06, 2009 (130)
13	1000GENOMES	ss109439166	Jan 24, 2009 (130)
14	1000GENOMES	ss113312505	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss116824791	Feb 14, 2009 (130)
16	ILLUMINA	ss122822802	Dec 01, 2009 (131)
17	ENSEMBL	ss139484938	Dec 01, 2009 (131)
18	ENSEMBL	ss143463677	Dec 01, 2009 (131)
19	ILLUMINA	ss154443568	Dec 01, 2009 (131)
20	GMI	ss156066190	Dec 01, 2009 (131)
21	ILLUMINA	ss159618480	Dec 01, 2009 (131)
22	ILLUMINA	ss160908587	Dec 01, 2009 (131)
23	COMPLETE_GENOMICS	ss162689480	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss165914643	Jul 04, 2010 (132)
25	ILLUMINA	ss172338946	Jul 04, 2010 (132)
26	ILLUMINA	ss174519947	Jul 04, 2010 (132)
27	BUSHMAN	ss200902234	Jul 04, 2010 (132)
28	BCM-HGSC-SUB	ss206739663	Jul 04, 2010 (132)
29	1000GENOMES	ss221981994	Jul 14, 2010 (132)
30	1000GENOMES	ss233160546	Jul 14, 2010 (132)
31	1000GENOMES	ss240279061	Jul 15, 2010 (132)
32	GMI	ss278492332	May 04, 2012 (137)
33	GMI	ss285267638	Apr 25, 2013 (138)
34	PJP	ss293465872	May 09, 2011 (134)
35	ILLUMINA	ss481657405	May 04, 2012 (137)
36	ILLUMINA	ss481688124	May 04, 2012 (137)
37	ILLUMINA	ss482654666	Sep 08, 2015 (146)
38	ILLUMINA	ss485623420	May 04, 2012 (137)
39	ILLUMINA	ss537507172	Sep 08, 2015 (146)
40	TISHKOFF	ss558731877	Apr 25, 2013 (138)
41	SSMP	ss652631031	Apr 25, 2013 (138)
42	ILLUMINA	ss778984252	Sep 08, 2015 (146)
43	ILLUMINA	ss783257311	Sep 08, 2015 (146)
44	ILLUMINA	ss784210813	Sep 08, 2015 (146)
45	ILLUMINA	ss825598593	Apr 01, 2015 (144)
46	ILLUMINA	ss832518184	Sep 08, 2015 (146)
47	ILLUMINA	ss833129408	Jul 13, 2019 (153)
48	ILLUMINA	ss834446437	Sep 08, 2015 (146)
49	EVA-GONL	ss982154529	Aug 21, 2014 (142)
50	JMKIDD_LAB	ss1073064443	Aug 21, 2014 (142)
51	1000GENOMES	ss1317335497	Aug 21, 2014 (142)
52	HAMMER_LAB	ss1397428508	Sep 08, 2015 (146)
53	DDI	ss1430511460	Apr 01, 2015 (144)
54	EVA_GENOME_DK	ss1581362547	Apr 01, 2015 (144)
55	EVA_UK10K_ALSPAC	ss1614075184	Apr 01, 2015 (144)
56	EVA_UK10K_TWINSUK	ss1657069217	Apr 01, 2015 (144)
57	EVA_SVP	ss1712802261	Apr 01, 2015 (144)
58	ILLUMINA	ss1752549688	Sep 08, 2015 (146)
59	HAMMER_LAB	ss1804094905	Sep 08, 2015 (146)
60	WEILL_CORNELL_DGM	ss1925411239	Feb 12, 2016 (147)
61	GENOMED	ss1970215048	Jul 19, 2016 (147)
62	JJLAB	ss2023311066	Sep 14, 2016 (149)
63	USC_VALOUEV	ss2151468231	Dec 20, 2016 (150)
64	HUMAN_LONGEVITY	ss2278402507	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2626143905	Nov 08, 2017 (151)
66	ILLUMINA	ss2634343395	Nov 08, 2017 (151)
67	ILLUMINA	ss2635149516	Nov 08, 2017 (151)
68	GRF	ss2707032231	Nov 08, 2017 (151)
69	GNOMAD	ss2831108861	Nov 08, 2017 (151)
70	SWEGEN	ss2997839126	Nov 08, 2017 (151)
71	BIOINF_KMB_FNS_UNIBA	ss3025438150	Nov 08, 2017 (151)
72	CSHL	ss3346641241	Nov 08, 2017 (151)
73	ILLUMINA	ss3629347118	Oct 12, 2018 (152)
74	ILLUMINA	ss3632267270	Oct 12, 2018 (152)
75	ILLUMINA	ss3633390783	Oct 12, 2018 (152)
76	ILLUMINA	ss3634112014	Oct 12, 2018 (152)
77	ILLUMINA	ss3635023039	Oct 12, 2018 (152)
78	ILLUMINA	ss3635793738	Oct 12, 2018 (152)
79	ILLUMINA	ss3636736649	Oct 12, 2018 (152)
80	ILLUMINA	ss3637546380	Oct 12, 2018 (152)
81	ILLUMINA	ss3638581985	Oct 12, 2018 (152)
82	ILLUMINA	ss3639293712	Oct 12, 2018 (152)
83	ILLUMINA	ss3639671101	Oct 12, 2018 (152)
84	ILLUMINA	ss3640730334	Oct 12, 2018 (152)
85	ILLUMINA	ss3641185571	Oct 12, 2018 (152)
86	ILLUMINA	ss3641482564	Oct 12, 2018 (152)
87	ILLUMINA	ss3643525829	Oct 12, 2018 (152)
88	URBANLAB	ss3648175147	Oct 12, 2018 (152)
89	EGCUT_WGS	ss3665753751	Jul 13, 2019 (153)
90	EVA_DECODE	ss3715758093	Jul 13, 2019 (153)
91	ACPOP	ss3732842058	Jul 13, 2019 (153)
92	ILLUMINA	ss3745323229	Jul 13, 2019 (153)
93	EVA	ss3764097010	Jul 13, 2019 (153)
94	ILLUMINA	ss3772817248	Jul 13, 2019 (153)
95	PACBIO	ss3785257341	Jul 13, 2019 (153)
96	PACBIO	ss3790639693	Jul 13, 2019 (153)
97	PACBIO	ss3795516643	Jul 13, 2019 (153)
98	KHV_HUMAN_GENOMES	ss3807271346	Jul 13, 2019 (153)
99	EVA	ss3829519067	Apr 26, 2020 (154)
100	EVA	ss3838233700	Apr 26, 2020 (154)
101	EVA	ss3843676341	Apr 26, 2020 (154)
102	HGDP	ss3847807899	Apr 26, 2020 (154)
103	SGDP_PRJ	ss3863038263	Apr 26, 2020 (154)
104	KRGDB	ss3909683628	Apr 26, 2020 (154)
105	KOGIC	ss3957701287	Apr 26, 2020 (154)
106	EVA	ss3985171869	Apr 26, 2021 (155)
107	TOPMED	ss4679739215	Apr 26, 2021 (155)
108	TOMMO_GENOMICS	ss5174271681	Apr 26, 2021 (155)
109	1000G_HIGH_COVERAGE	ss5265947960	Oct 13, 2022 (156)
110	EVA	ss5315088156	Oct 13, 2022 (156)
111	EVA	ss5361155447	Oct 13, 2022 (156)
112	HUGCELL_USP	ss5463904691	Oct 13, 2022 (156)
113	EVA	ss5508225786	Oct 13, 2022 (156)
114	1000G_HIGH_COVERAGE	ss5550648586	Oct 13, 2022 (156)
115	SANFORD_IMAGENETICS	ss5638942678	Oct 13, 2022 (156)
116	TOMMO_GENOMICS	ss5711386952	Oct 13, 2022 (156)
117	EVA	ss5799662952	Oct 13, 2022 (156)
118	YY_MCH	ss5806790613	Oct 13, 2022 (156)
119	EVA	ss5835681993	Oct 13, 2022 (156)
120	EVA	ss5855029498	Oct 13, 2022 (156)
121	EVA	ss5896441704	Oct 13, 2022 (156)
122	EVA	ss5967411600	Oct 13, 2022 (156)
123	EVA	ss5980318028	Oct 13, 2022 (156)
124	1000Genomes	NC_000005.9 - 134939703	Oct 12, 2018 (152)
125	1000Genomes_30x	NC_000005.10 - 135604013	Oct 13, 2022 (156)
126	The Avon Longitudinal Study of Parents and Children	NC_000005.9 - 134939703	Oct 12, 2018 (152)
127	Genome-wide autozygosity in Daghestan	NC_000005.8 - 134967602	Apr 26, 2020 (154)
128	Genetic variation in the Estonian population	NC_000005.9 - 134939703	Oct 12, 2018 (152)
129	The Danish reference pan genome	NC_000005.9 - 134939703	Apr 26, 2020 (154)
130	gnomAD - Genomes	NC_000005.10 - 135604013	Apr 26, 2021 (155)
131	Genome of the Netherlands Release 5	NC_000005.9 - 134939703	Apr 26, 2020 (154)
132	HGDP-CEPH-db Supplement 1	NC_000005.8 - 134967602	Apr 26, 2020 (154)
133	HapMap	NC_000005.10 - 135604013	Apr 26, 2020 (154)
134	KOREAN population from KRGDB	NC_000005.9 - 134939703	Apr 26, 2020 (154)
135	Korean Genome Project	NC_000005.10 - 135604013	Apr 26, 2020 (154)
136	Northern Sweden	NC_000005.9 - 134939703	Jul 13, 2019 (153)
137	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000005.9 - 134939703	Apr 26, 2021 (155)
138	Qatari	NC_000005.9 - 134939703	Apr 26, 2020 (154)
139	SGDP_PRJ	NC_000005.9 - 134939703	Apr 26, 2020 (154)
140	Siberian	NC_000005.9 - 134939703	Apr 26, 2020 (154)
141	8.3KJPN	NC_000005.9 - 134939703	Apr 26, 2021 (155)
142	14KJPN	NC_000005.10 - 135604013	Oct 13, 2022 (156)
143	TopMed	NC_000005.10 - 135604013	Apr 26, 2021 (155)
144	UK 10K study - Twins	NC_000005.9 - 134939703	Oct 12, 2018 (152)
145	A Vietnamese Genetic Variation Database	NC_000005.9 - 134939703	Jul 13, 2019 (153)
146	ALFA	NC_000005.10 - 135604013	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)
rs61533917	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
16861022, ss3909683628	NC_000005.9:134939702:T:A	NC_000005.10:135604012:T:A	(self)
12110599585	NC_000005.10:135604012:T:A	NC_000005.10:135604012:T:A	(self)
403357, 485791, ss93259854, ss109439166, ss113312505, ss116824791, ss162689480, ss165914643, ss200902234, ss206739663, ss278492332, ss285267638, ss293465872, ss481657405, ss825598593, ss1397428508, ss1712802261, ss2635149516, ss3639293712, ss3639671101, ss3643525829, ss3847807899	NC_000005.8:134967601:T:C	NC_000005.10:135604012:T:C	(self)
29018252, 16140741, 11491999, 7527486, 7172782, 16861022, 6126923, 397796, 7453169, 15055243, 3984585, 32240988, 16140741, 3579386, ss221981994, ss233160546, ss240279061, ss481688124, ss482654666, ss485623420, ss537507172, ss558731877, ss652631031, ss778984252, ss783257311, ss784210813, ss832518184, ss833129408, ss834446437, ss982154529, ss1073064443, ss1317335497, ss1430511460, ss1581362547, ss1614075184, ss1657069217, ss1752549688, ss1804094905, ss1925411239, ss1970215048, ss2023311066, ss2151468231, ss2626143905, ss2634343395, ss2707032231, ss2831108861, ss2997839126, ss3346641241, ss3629347118, ss3632267270, ss3633390783, ss3634112014, ss3635023039, ss3635793738, ss3636736649, ss3637546380, ss3638581985, ss3640730334, ss3641185571, ss3641482564, ss3665753751, ss3732842058, ss3745323229, ss3764097010, ss3772817248, ss3785257341, ss3790639693, ss3795516643, ss3829519067, ss3838233700, ss3863038263, ss3909683628, ss3985171869, ss5174271681, ss5315088156, ss5361155447, ss5508225786, ss5638942678, ss5799662952, ss5835681993, ss5967411600, ss5980318028	NC_000005.9:134939702:T:C	NC_000005.10:135604012:T:C	(self)
38174521, 205233022, 2974024, 14079288, 45224056, 517116772, 12110599585, ss2278402507, ss3025438150, ss3648175147, ss3715758093, ss3807271346, ss3843676341, ss3957701287, ss4679739215, ss5265947960, ss5463904691, ss5550648586, ss5711386952, ss5806790613, ss5855029498, ss5896441704	NC_000005.10:135604012:T:C	NC_000005.10:135604012:T:C	(self)
ss11758688	NT_034772.4:37354723:T:C	NC_000005.10:135604012:T:C	(self)
ss42640441, ss66788174, ss67823812, ss67986887, ss70946379, ss71551408, ss75766849, ss79268075, ss84715054, ss98767261, ss122822802, ss139484938, ss143463677, ss154443568, ss156066190, ss159618480, ss160908587, ss172338946, ss174519947	NT_034772.6:43253574:T:C	NC_000005.10:135604012:T:C	(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 rs7732567

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

rs7732567