Name: rs7571337
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.

rs7571337

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:233657772 (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>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.451245 (119440/264690, TOPMED)
C=0.484605 (101425/209294, ALFA)
T=0.41520 (11732/28256, 14KJPN) (+ 20 more)
T=0.41891 (7021/16760, 8.3KJPN)
T=0.4586 (2937/6404, 1000G_30x)
T=0.4641 (2324/5008, 1000G)
T=0.4908 (2199/4480, Estonian)
T=0.4886 (1883/3854, ALSPAC)
T=0.4916 (1823/3708, TWINSUK)
T=0.4369 (1280/2930, KOREAN)
C=0.4880 (1017/2084, HGDP_Stanford)
T=0.4279 (807/1886, HapMap)
T=0.4498 (824/1832, Korea1K)
T=0.482 (481/998, GoNL)
T=0.476 (375/788, PRJEB37584)
C=0.478 (287/600, NorthernSweden)
T=0.292 (124/424, SGDP_PRJ)
T=0.384 (83/216, Qatari)
T=0.468 (101/216, Vietnamese)
T=0.32 (14/44, Siberian)
T=0.30 (12/40, GENOME_DK)
T=0.50 (18/36, Ancient Sardinia)
C=0.50 (18/36, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UGT1A10 : Intron Variant
UGT1A8 : Intron Variant
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	209294	T=0.515395	C=0.484605, G=0.000000
European	Sub	185304	T=0.516486	C=0.483514, G=0.000000
African	Sub	4626	T=0.3898	C=0.6102, G=0.0000
African Others	Sub	168	T=0.375	C=0.625, G=0.000
African American	Sub	4458	T=0.3903	C=0.6097, G=0.0000
Asian	Sub	666	T=0.497	C=0.503, G=0.000
East Asian	Sub	538	T=0.485	C=0.515, G=0.000
Other Asian	Sub	128	T=0.547	C=0.453, G=0.000
Latin American 1	Sub	736	T=0.408	C=0.592, G=0.000
Latin American 2	Sub	6434	T=0.5267	C=0.4733, G=0.0000
South Asian	Sub	4982	T=0.6116	C=0.3884, G=0.0000
Other	Sub	6546	T=0.5029	C=0.4971, G=0.0000

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=0.451245	C=0.548755
Allele Frequency Aggregator	Total	Global	209294	T=0.515395	C=0.484605, G=0.000000
Allele Frequency Aggregator	European	Sub	185304	T=0.516486	C=0.483514, G=0.000000
Allele Frequency Aggregator	Other	Sub	6546	T=0.5029	C=0.4971, G=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	6434	T=0.5267	C=0.4733, G=0.0000
Allele Frequency Aggregator	South Asian	Sub	4982	T=0.6116	C=0.3884, G=0.0000
Allele Frequency Aggregator	African	Sub	4626	T=0.3898	C=0.6102, G=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	736	T=0.408	C=0.592, G=0.000
Allele Frequency Aggregator	Asian	Sub	666	T=0.497	C=0.503, G=0.000
14KJPN	JAPANESE	Study-wide	28256	T=0.41520	C=0.58480
8.3KJPN	JAPANESE	Study-wide	16760	T=0.41891	C=0.58109
1000Genomes_30x	Global	Study-wide	6404	T=0.4586	C=0.5414
1000Genomes_30x	African	Sub	1786	T=0.3001	C=0.6999
1000Genomes_30x	Europe	Sub	1266	T=0.5047	C=0.4953
1000Genomes_30x	South Asian	Sub	1202	T=0.6106	C=0.3894
1000Genomes_30x	East Asian	Sub	1170	T=0.4701	C=0.5299
1000Genomes_30x	American	Sub	980	T=0.488	C=0.512
1000Genomes	Global	Study-wide	5008	T=0.4641	C=0.5359
1000Genomes	African	Sub	1322	T=0.2995	C=0.7005
1000Genomes	East Asian	Sub	1008	T=0.4603	C=0.5397
1000Genomes	Europe	Sub	1006	T=0.5159	C=0.4841
1000Genomes	South Asian	Sub	978	T=0.620	C=0.380
1000Genomes	American	Sub	694	T=0.488	C=0.512
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.4908	C=0.5092
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.4886	C=0.5114
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.4916	C=0.5084
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.4369	C=0.5631
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.5120	C=0.4880
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.513	C=0.487
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.611	C=0.389
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.543	C=0.457
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.531	C=0.469
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.306	C=0.694
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.509	C=0.491
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.40	C=0.60
HapMap	Global	Study-wide	1886	T=0.4279	C=0.5721
HapMap	American	Sub	768	T=0.492	C=0.508
HapMap	African	Sub	690	T=0.325	C=0.675
HapMap	Asian	Sub	252	T=0.452	C=0.548
HapMap	Europe	Sub	176	T=0.517	C=0.483
Korean Genome Project	KOREAN	Study-wide	1832	T=0.4498	C=0.5502
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.482	C=0.518
CNV burdens in cranial meningiomas	Global	Study-wide	788	T=0.476	C=0.524
CNV burdens in cranial meningiomas	CRM	Sub	788	T=0.476	C=0.524
Northern Sweden	ACPOP	Study-wide	600	T=0.522	C=0.478
SGDP_PRJ	Global	Study-wide	424	T=0.292	C=0.708
Qatari	Global	Study-wide	216	T=0.384	C=0.616
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.468	C=0.532
Siberian	Global	Study-wide	44	T=0.32	C=0.68
The Danish reference pan genome	Danish	Study-wide	40	T=0.30	C=0.70
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	36	T=0.50	C=0.50

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 2	NC_000002.12:g.233657772T>C
GRCh38.p14 chr 2	NC_000002.12:g.233657772T>G
GRCh37.p13 chr 2	NC_000002.11:g.234566418T>C
GRCh37.p13 chr 2	NC_000002.11:g.234566418T>G
UGT1A RefSeqGene	NG_002601.2:g.73029T>C
UGT1A RefSeqGene	NG_002601.2:g.73029T>G

Gene: UGT1A10, UDP glucuronosyltransferase family 1 member A10 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UGT1A10 transcript	NM_019075.4:c.855+20395T>C	N/A	Intron Variant

Gene: UGT1A8, UDP glucuronosyltransferase family 1 member A8 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UGT1A8 transcript	NM_019076.5:c.855+39210T>C	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.

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=	C	G
GRCh38.p14 chr 2	NC_000002.12:g.233657772=	NC_000002.12:g.233657772T>C	NC_000002.12:g.233657772T>G
GRCh37.p13 chr 2	NC_000002.11:g.234566418=	NC_000002.11:g.234566418T>C	NC_000002.11:g.234566418T>G
UGT1A RefSeqGene	NG_002601.2:g.73029=	NG_002601.2:g.73029T>C	NG_002601.2:g.73029T>G
UGT1A10 transcript	NM_019075.2:c.855+20395=	NM_019075.2:c.855+20395T>C	NM_019075.2:c.855+20395T>G
UGT1A10 transcript	NM_019075.4:c.855+20395=	NM_019075.4:c.855+20395T>C	NM_019075.4:c.855+20395T>G
UGT1A8 transcript	NM_019076.4:c.855+39210=	NM_019076.4:c.855+39210T>C	NM_019076.4:c.855+39210T>G
UGT1A8 transcript	NM_019076.5:c.855+39210=	NM_019076.5:c.855+39210T>C	NM_019076.5:c.855+39210T>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#.

118 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11459121	Jul 11, 2003 (116)
2	KRIBB_YJKIM	ss65833341	Nov 30, 2006 (127)
3	ILLUMINA	ss66691511	Nov 30, 2006 (127)
4	ILLUMINA	ss67800252	Nov 30, 2006 (127)
5	ILLUMINA	ss67972465	Nov 30, 2006 (127)
6	PERLEGEN	ss68846564	May 17, 2007 (127)
7	ILLUMINA	ss70934562	May 23, 2008 (130)
8	ILLUMINA	ss71536973	May 17, 2007 (127)
9	ILLUMINA	ss75557717	Dec 07, 2007 (129)
10	HGSV	ss77826618	Dec 07, 2007 (129)
11	ILLUMINA	ss79261132	Dec 14, 2007 (130)
12	KRIBB_YJKIM	ss84681331	Dec 14, 2007 (130)
13	HUMANGENOME_JCVI	ss97131918	Feb 04, 2009 (130)
14	BGI	ss106168900	Feb 04, 2009 (130)
15	1000GENOMES	ss110964105	Jan 25, 2009 (130)
16	ILLUMINA-UK	ss118122733	Feb 14, 2009 (130)
17	ILLUMINA	ss122781349	Dec 01, 2009 (131)
18	ENSEMBL	ss143308133	Dec 01, 2009 (131)
19	ILLUMINA	ss154431095	Dec 01, 2009 (131)
20	GMI	ss154867384	Dec 01, 2009 (131)
21	ILLUMINA	ss159606191	Dec 01, 2009 (131)
22	ILLUMINA	ss160890011	Dec 01, 2009 (131)
23	COMPLETE_GENOMICS	ss165963729	Jul 04, 2010 (132)
24	ILLUMINA	ss172308585	Jul 04, 2010 (132)
25	ILLUMINA	ss174425126	Jul 04, 2010 (132)
26	BUSHMAN	ss201894603	Jul 04, 2010 (132)
27	1000GENOMES	ss211106309	Jul 14, 2010 (132)
28	1000GENOMES	ss219880667	Jul 14, 2010 (132)
29	1000GENOMES	ss231635226	Jul 14, 2010 (132)
30	1000GENOMES	ss239082872	Jul 15, 2010 (132)
31	BL	ss253935062	May 09, 2011 (134)
32	GMI	ss276943821	May 04, 2012 (137)
33	GMI	ss284563045	Apr 25, 2013 (138)
34	PJP	ss292510726	May 09, 2011 (134)
35	ILLUMINA	ss481599732	May 04, 2012 (137)
36	ILLUMINA	ss481629697	May 04, 2012 (137)
37	ILLUMINA	ss482598893	Sep 08, 2015 (146)
38	ILLUMINA	ss485594785	May 04, 2012 (137)
39	ILLUMINA	ss537484334	Sep 08, 2015 (146)
40	TISHKOFF	ss556304796	Apr 25, 2013 (138)
41	SSMP	ss649965648	Apr 25, 2013 (138)
42	ILLUMINA	ss778978091	Sep 08, 2015 (146)
43	ILLUMINA	ss783242977	Sep 08, 2015 (146)
44	ILLUMINA	ss784196749	Sep 08, 2015 (146)
45	ILLUMINA	ss825591650	Apr 01, 2015 (144)
46	ILLUMINA	ss832503578	Sep 08, 2015 (146)
47	ILLUMINA	ss833117175	Jul 13, 2019 (153)
48	ILLUMINA	ss834440210	Sep 08, 2015 (146)
49	EVA-GONL	ss978087715	Aug 21, 2014 (142)
50	JMKIDD_LAB	ss1070035592	Aug 21, 2014 (142)
51	1000GENOMES	ss1302131276	Aug 21, 2014 (142)
52	DDI	ss1428949759	Apr 01, 2015 (144)
53	EVA_GENOME_DK	ss1579373208	Apr 01, 2015 (144)
54	EVA_DECODE	ss1587547857	Apr 01, 2015 (144)
55	EVA_UK10K_ALSPAC	ss1606056048	Apr 01, 2015 (144)
56	EVA_UK10K_TWINSUK	ss1649050081	Apr 01, 2015 (144)
57	EVA_SVP	ss1712539784	Apr 01, 2015 (144)
58	ILLUMINA	ss1752345035	Sep 08, 2015 (146)
59	HAMMER_LAB	ss1798565739	Sep 08, 2015 (146)
60	WEILL_CORNELL_DGM	ss1921335373	Feb 12, 2016 (147)
61	GENOMED	ss1969055391	Jul 19, 2016 (147)
62	JJLAB	ss2021215922	Sep 14, 2016 (149)
63	USC_VALOUEV	ss2149282074	Dec 20, 2016 (150)
64	HUMAN_LONGEVITY	ss2240157402	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2625108160	Nov 08, 2017 (151)
66	ILLUMINA	ss2633755196	Nov 08, 2017 (151)
67	GRF	ss2703934707	Nov 08, 2017 (151)
68	ILLUMINA	ss2710928775	Nov 08, 2017 (151)
69	GNOMAD	ss2787703282	Nov 08, 2017 (151)
70	SWEGEN	ss2991557116	Nov 08, 2017 (151)
71	BIOINF_KMB_FNS_UNIBA	ss3024368123	Nov 08, 2017 (151)
72	CSHL	ss3344798100	Nov 08, 2017 (151)
73	ILLUMINA	ss3628313892	Oct 11, 2018 (152)
74	ILLUMINA	ss3631714424	Oct 11, 2018 (152)
75	ILLUMINA	ss3633238406	Oct 11, 2018 (152)
76	ILLUMINA	ss3633951797	Oct 11, 2018 (152)
77	ILLUMINA	ss3634818031	Oct 11, 2018 (152)
78	ILLUMINA	ss3635637156	Oct 11, 2018 (152)
79	ILLUMINA	ss3636508123	Oct 11, 2018 (152)
80	ILLUMINA	ss3637389187	Oct 11, 2018 (152)
81	ILLUMINA	ss3638325469	Oct 11, 2018 (152)
82	ILLUMINA	ss3639166131	Oct 11, 2018 (152)
83	ILLUMINA	ss3639596735	Oct 11, 2018 (152)
84	ILLUMINA	ss3640525330	Oct 11, 2018 (152)
85	ILLUMINA	ss3643289662	Oct 11, 2018 (152)
86	URBANLAB	ss3647302618	Oct 11, 2018 (152)
87	EGCUT_WGS	ss3659455250	Jul 13, 2019 (153)
88	EVA_DECODE	ss3706264853	Jul 13, 2019 (153)
89	ACPOP	ss3729480309	Jul 13, 2019 (153)
90	ILLUMINA	ss3745117923	Jul 13, 2019 (153)
91	EVA	ss3758233643	Jul 13, 2019 (153)
92	ILLUMINA	ss3772614301	Jul 13, 2019 (153)
93	PACBIO	ss3784187773	Jul 13, 2019 (153)
94	PACBIO	ss3789721144	Jul 13, 2019 (153)
95	PACBIO	ss3794594589	Jul 13, 2019 (153)
96	KHV_HUMAN_GENOMES	ss3802596132	Jul 13, 2019 (153)
97	EVA	ss3827569415	Apr 25, 2020 (154)
98	HGDP	ss3847655015	Apr 25, 2020 (154)
99	SGDP_PRJ	ss3854852335	Apr 25, 2020 (154)
100	KRGDB	ss3900601238	Apr 25, 2020 (154)
101	KOGIC	ss3950333918	Apr 25, 2020 (154)
102	EVA	ss3984499888	Apr 27, 2021 (155)
103	EVA	ss3984961442	Apr 27, 2021 (155)
104	TOPMED	ss4548808046	Apr 27, 2021 (155)
105	TOMMO_GENOMICS	ss5157052578	Apr 27, 2021 (155)
106	1000G_HIGH_COVERAGE	ss5252460376	Oct 13, 2022 (156)
107	EVA	ss5314817461	Oct 13, 2022 (156)
108	EVA	ss5336818470	Oct 13, 2022 (156)
109	HUGCELL_USP	ss5452028836	Oct 13, 2022 (156)
110	1000G_HIGH_COVERAGE	ss5530015211	Oct 13, 2022 (156)
111	SANFORD_IMAGENETICS	ss5631196696	Oct 13, 2022 (156)
112	TOMMO_GENOMICS	ss5688103450	Oct 13, 2022 (156)
113	EVA	ss5799563740	Oct 13, 2022 (156)
114	YY_MCH	ss5803327343	Oct 13, 2022 (156)
115	EVA	ss5821759130	Oct 13, 2022 (156)
116	EVA	ss5853001251	Oct 13, 2022 (156)
117	EVA	ss5935198085	Oct 13, 2022 (156)
118	EVA	ss5957462275	Oct 13, 2022 (156)
119	1000Genomes	NC_000002.11 - 234566418	Oct 11, 2018 (152)
120	1000Genomes_30x	NC_000002.12 - 233657772	Oct 13, 2022 (156)
121	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 234566418	Oct 11, 2018 (152)
122	Genetic variation in the Estonian population	NC_000002.11 - 234566418	Oct 11, 2018 (152)
123	The Danish reference pan genome	NC_000002.11 - 234566418	Apr 25, 2020 (154)
124	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94440127 (NC_000002.12:233657771:T:C 75509/140004) Row 94440128 (NC_000002.12:233657771:T:G 1/140050)	-	Apr 27, 2021 (155)
125	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94440127 (NC_000002.12:233657771:T:C 75509/140004) Row 94440128 (NC_000002.12:233657771:T:G 1/140050)	-	Apr 27, 2021 (155)
126	Genome of the Netherlands Release 5	NC_000002.11 - 234566418	Apr 25, 2020 (154)
127	HGDP-CEPH-db Supplement 1	NC_000002.10 - 234231157	Apr 25, 2020 (154)
128	HapMap	NC_000002.12 - 233657772	Apr 25, 2020 (154)
129	KOREAN population from KRGDB	NC_000002.11 - 234566418	Apr 25, 2020 (154)
130	Korean Genome Project	NC_000002.12 - 233657772	Apr 25, 2020 (154)
131	Northern Sweden	NC_000002.11 - 234566418	Jul 13, 2019 (153)
132	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000002.11 - 234566418	Apr 27, 2021 (155)
133	CNV burdens in cranial meningiomas	NC_000002.11 - 234566418	Apr 27, 2021 (155)
134	Qatari	NC_000002.11 - 234566418	Apr 25, 2020 (154)
135	SGDP_PRJ	NC_000002.11 - 234566418	Apr 25, 2020 (154)
136	Siberian	NC_000002.11 - 234566418	Apr 25, 2020 (154)
137	8.3KJPN	NC_000002.11 - 234566418	Apr 27, 2021 (155)
138	14KJPN	NC_000002.12 - 233657772	Oct 13, 2022 (156)
139	TopMed	NC_000002.12 - 233657772	Apr 27, 2021 (155)
140	UK 10K study - Twins	NC_000002.11 - 234566418	Oct 11, 2018 (152)
141	A Vietnamese Genetic Variation Database	NC_000002.11 - 234566418	Jul 13, 2019 (153)
142	ALFA	NC_000002.12 - 233657772	Apr 27, 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)
rs57218657	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77826618, ss3639166131, ss3639596735	NC_000002.9:234348417:T:C	NC_000002.12:233657771:T:C	(self)
332907, ss110964105, ss118122733, ss165963729, ss201894603, ss211106309, ss253935062, ss276943821, ss284563045, ss292510726, ss481599732, ss825591650, ss1587547857, ss1712539784, ss3643289662, ss3847655015	NC_000002.10:234231156:T:C	NC_000002.12:233657771:T:C	(self)
13254326, 7341195, 5193498, 5538147, 3216232, 7778632, 2765174, 187369, 49226, 3377303, 6869315, 1798428, 15021885, 7341195, 1593633, ss219880667, ss231635226, ss239082872, ss481629697, ss482598893, ss485594785, ss537484334, ss556304796, ss649965648, ss778978091, ss783242977, ss784196749, ss832503578, ss833117175, ss834440210, ss978087715, ss1070035592, ss1302131276, ss1428949759, ss1579373208, ss1606056048, ss1649050081, ss1752345035, ss1798565739, ss1921335373, ss1969055391, ss2021215922, ss2149282074, ss2625108160, ss2633755196, ss2703934707, ss2710928775, ss2787703282, ss2991557116, ss3344798100, ss3628313892, ss3631714424, ss3633238406, ss3633951797, ss3634818031, ss3635637156, ss3636508123, ss3637389187, ss3638325469, ss3640525330, ss3659455250, ss3729480309, ss3745117923, ss3758233643, ss3772614301, ss3784187773, ss3789721144, ss3794594589, ss3827569415, ss3854852335, ss3900601238, ss3984499888, ss3984961442, ss5157052578, ss5314817461, ss5336818470, ss5631196696, ss5799563740, ss5821759130, ss5957462275	NC_000002.11:234566417:T:C	NC_000002.12:233657771:T:C	(self)
17541146, 2034819, 6711919, 21940554, 352630925, 13460302681, ss2240157402, ss3024368123, ss3647302618, ss3706264853, ss3802596132, ss3950333918, ss4548808046, ss5252460376, ss5452028836, ss5530015211, ss5688103450, ss5803327343, ss5853001251, ss5935198085	NC_000002.12:233657771:T:C	NC_000002.12:233657771:T:C	(self)
ss11459121	NT_005120.13:496951:T:C	NC_000002.12:233657771:T:C	(self)
ss65833341, ss66691511, ss67800252, ss67972465, ss68846564, ss70934562, ss71536973, ss75557717, ss79261132, ss84681331, ss97131918, ss106168900, ss122781349, ss143308133, ss154431095, ss154867384, ss159606191, ss160890011, ss172308585, ss174425126	NT_005120.16:512676:T:C	NC_000002.12:233657771:T:C	(self)
13460302681	NC_000002.12:233657771:T:G	NC_000002.12:233657771:T:G	(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 rs7571337

PMID	Title	Author	Year	Journal
23632476	Fluid intake, genetic variants of UDP-glucuronosyltransferases, and bladder cancer risk.	Wang J et al.	2013	British journal of cancer

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

rs7571337