Name: rs6671188
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.

rs6671188

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:155741860 (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=0.026692 (7065/264690, TOPMED)
T=0.038042 (6014/158088, ALFA)
T=0.025645 (3595/140186, GnomAD) (+ 18 more)
T=0.00007 (2/28256, 14KJPN)
T=0.00012 (2/16760, 8.3KJPN)
T=0.0178 (114/6404, 1000G_30x)
T=0.0178 (89/5008, 1000G)
T=0.0371 (143/3854, ALSPAC)
T=0.0396 (147/3708, TWINSUK)
T=0.0000 (0/2930, KOREAN)
A=0.0000 (0/2930, KOREAN)
G=0.0000 (0/2930, KOREAN)
T=0.0000 (0/1832, Korea1K)
T=0.0341 (40/1172, HapMap)
T=0.035 (35/998, GoNL)
T=0.013 (8/600, NorthernSweden)
T=0.016 (9/556, SGDP_PRJ)
T=0.051 (11/216, Qatari)
T=0.009 (2/214, Vietnamese)
T=0.00 (0/56, Siberian)
T=0.00 (0/40, GENOME_DK)

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	158088	T=0.038042	A=0.000000, C=0.961958
European	Sub	137728	T=0.040631	A=0.000000, C=0.959369
African	Sub	6160	T=0.0055	A=0.0000, C=0.9945
African Others	Sub	218	T=0.000	A=0.000, C=1.000
African American	Sub	5942	T=0.0057	A=0.0000, C=0.9943
Asian	Sub	636	T=0.000	A=0.000, C=1.000
East Asian	Sub	504	T=0.000	A=0.000, C=1.000
Other Asian	Sub	132	T=0.000	A=0.000, C=1.000
Latin American 1	Sub	758	T=0.025	A=0.000, C=0.975
Latin American 2	Sub	6346	T=0.0263	A=0.0000, C=0.9737
South Asian	Sub	184	T=0.016	A=0.000, C=0.984
Other	Sub	6276	T=0.0311	A=0.0000, C=0.9689

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	T=0.026692	C=0.973308
Allele Frequency Aggregator	Total	Global	158088	T=0.038042	A=0.000000, C=0.961958
Allele Frequency Aggregator	European	Sub	137728	T=0.040631	A=0.000000, C=0.959369
Allele Frequency Aggregator	Latin American 2	Sub	6346	T=0.0263	A=0.0000, C=0.9737
Allele Frequency Aggregator	Other	Sub	6276	T=0.0311	A=0.0000, C=0.9689
Allele Frequency Aggregator	African	Sub	6160	T=0.0055	A=0.0000, C=0.9945
Allele Frequency Aggregator	Latin American 1	Sub	758	T=0.025	A=0.000, C=0.975
Allele Frequency Aggregator	Asian	Sub	636	T=0.000	A=0.000, C=1.000
Allele Frequency Aggregator	South Asian	Sub	184	T=0.016	A=0.000, C=0.984
gnomAD - Genomes	Global	Study-wide	140186	T=0.025645	C=0.974355
gnomAD - Genomes	European	Sub	75940	T=0.03359	C=0.96641
gnomAD - Genomes	African	Sub	42006	T=0.00712	C=0.99288
gnomAD - Genomes	American	Sub	13640	T=0.03174	C=0.96826
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.0753	C=0.9247
gnomAD - Genomes	East Asian	Sub	3134	T=0.0006	C=0.9994
gnomAD - Genomes	Other	Sub	2146	T=0.0280	C=0.9720
14KJPN	JAPANESE	Study-wide	28256	T=0.00007	C=0.99993
8.3KJPN	JAPANESE	Study-wide	16760	T=0.00012	C=0.99988
1000Genomes_30x	Global	Study-wide	6404	T=0.0178	C=0.9822
1000Genomes_30x	African	Sub	1786	T=0.0000	C=1.0000
1000Genomes_30x	Europe	Sub	1266	T=0.0324	C=0.9676
1000Genomes_30x	South Asian	Sub	1202	T=0.0308	C=0.9692
1000Genomes_30x	East Asian	Sub	1170	T=0.0000	C=1.0000
1000Genomes_30x	American	Sub	980	T=0.037	C=0.963
1000Genomes	Global	Study-wide	5008	T=0.0178	C=0.9822
1000Genomes	African	Sub	1322	T=0.0000	C=1.0000
1000Genomes	East Asian	Sub	1008	T=0.0000	C=1.0000
1000Genomes	Europe	Sub	1006	T=0.0308	C=0.9692
1000Genomes	South Asian	Sub	978	T=0.031	C=0.969
1000Genomes	American	Sub	694	T=0.040	C=0.960
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.0371	C=0.9629
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.0396	C=0.9604
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.0000	A=0.0000, C=1.0000, G=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	T=0.0000	C=1.0000
HapMap	Global	Study-wide	1172	T=0.0341	C=0.9659
HapMap	American	Sub	502	T=0.038	C=0.962
HapMap	African	Sub	406	T=0.025	C=0.975
HapMap	Europe	Sub	176	T=0.062	C=0.938
HapMap	Asian	Sub	88	T=0.00	C=1.00
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.035	C=0.965
Northern Sweden	ACPOP	Study-wide	600	T=0.013	C=0.987
SGDP_PRJ	Global	Study-wide	556	T=0.016	C=0.984
Qatari	Global	Study-wide	216	T=0.051	C=0.949
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.009	C=0.991
Siberian	Global	Study-wide	56	T=0.00	C=1.00
The Danish reference pan genome	Danish	Study-wide	40	T=0.00	C=1.00

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 1	NC_000001.11:g.155741860T>A
GRCh38.p14 chr 1	NC_000001.11:g.155741860T>C
GRCh38.p14 chr 1	NC_000001.11:g.155741860T>G
GRCh37.p13 chr 1	NC_000001.10:g.155711651T>A
GRCh37.p13 chr 1	NC_000001.10:g.155711651T>C
GRCh37.p13 chr 1	NC_000001.10:g.155711651T>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 1	NC_000001.11:g.155741860=	NC_000001.11:g.155741860T>A	NC_000001.11:g.155741860T>C	NC_000001.11:g.155741860T>G
GRCh37.p13 chr 1	NC_000001.10:g.155711651=	NC_000001.10:g.155711651T>A	NC_000001.10:g.155711651T>C	NC_000001.10:g.155711651T>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#.

115 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss9838527	Jul 11, 2003 (116)
2	CSHL-HAPMAP	ss16388853	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss19098844	Feb 27, 2004 (120)
4	SSAHASNP	ss20473269	Apr 05, 2004 (121)
5	ABI	ss43837850	Mar 14, 2006 (126)
6	ILLUMINA	ss75323586	Dec 07, 2007 (129)
7	HGSV	ss78154661	Dec 07, 2007 (129)
8	BCMHGSC_JDW	ss87826335	Mar 23, 2008 (129)
9	HUMANGENOME_JCVI	ss97975260	Feb 05, 2009 (130)
10	BGI	ss106602395	Feb 05, 2009 (130)
11	1000GENOMES	ss108603527	Jan 23, 2009 (130)
12	1000GENOMES	ss111163281	Jan 25, 2009 (130)
13	ILLUMINA-UK	ss119034954	Dec 01, 2009 (131)
14	KRIBB_YJKIM	ss119520070	Dec 01, 2009 (131)
15	ILLUMINA	ss123461915	Dec 01, 2009 (131)
16	ENSEMBL	ss131696237	Dec 01, 2009 (131)
17	ENSEMBL	ss138084293	Dec 01, 2009 (131)
18	ILLUMINA	ss154374245	Dec 01, 2009 (131)
19	GMI	ss155760240	Dec 01, 2009 (131)
20	ILLUMINA	ss160796269	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss164133122	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss165230315	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss167139347	Jul 04, 2010 (132)
24	ILLUMINA	ss172168445	Jul 04, 2010 (132)
25	ILLUMINA	ss174062908	Jul 04, 2010 (132)
26	BUSHMAN	ss199093827	Jul 04, 2010 (132)
27	BCM-HGSC-SUB	ss205068784	Jul 04, 2010 (132)
28	1000GENOMES	ss218654024	Jul 14, 2010 (132)
29	1000GENOMES	ss230733918	Jul 14, 2010 (132)
30	1000GENOMES	ss238381187	Jul 15, 2010 (132)
31	BL	ss253512861	May 09, 2011 (134)
32	GMI	ss276053159	May 04, 2012 (137)
33	GMI	ss284153512	Apr 25, 2013 (138)
34	PJP	ss290638145	May 09, 2011 (134)
35	ILLUMINA	ss481311786	May 04, 2012 (137)
36	ILLUMINA	ss481336841	May 04, 2012 (137)
37	ILLUMINA	ss482319017	Sep 08, 2015 (146)
38	ILLUMINA	ss485451079	May 04, 2012 (137)
39	ILLUMINA	ss537376418	Sep 08, 2015 (146)
40	TISHKOFF	ss554706000	Apr 25, 2013 (138)
41	SSMP	ss648418042	Apr 25, 2013 (138)
42	ILLUMINA	ss778575787	Aug 21, 2014 (142)
43	ILLUMINA	ss783170988	Aug 21, 2014 (142)
44	ILLUMINA	ss784126531	Aug 21, 2014 (142)
45	ILLUMINA	ss825677783	Apr 01, 2015 (144)
46	ILLUMINA	ss832430531	Apr 01, 2015 (144)
47	ILLUMINA	ss834032862	Aug 21, 2014 (142)
48	EVA-GONL	ss975689357	Aug 21, 2014 (142)
49	JMKIDD_LAB	ss1068273582	Aug 21, 2014 (142)
50	1000GENOMES	ss1292954461	Aug 21, 2014 (142)
51	DDI	ss1425980192	Apr 01, 2015 (144)
52	EVA_GENOME_DK	ss1574395305	Apr 01, 2015 (144)
53	EVA_DECODE	ss1585071122	Apr 01, 2015 (144)
54	EVA_UK10K_ALSPAC	ss1601228649	Apr 01, 2015 (144)
55	EVA_UK10K_TWINSUK	ss1644222682	Apr 01, 2015 (144)
56	EVA_SVP	ss1712371401	Apr 01, 2015 (144)
57	ILLUMINA	ss1751872976	Sep 08, 2015 (146)
58	HAMMER_LAB	ss1795100536	Sep 08, 2015 (146)
59	WEILL_CORNELL_DGM	ss1918923007	Feb 12, 2016 (147)
60	GENOMED	ss1966868565	Jul 19, 2016 (147)
61	JJLAB	ss2019976626	Sep 14, 2016 (149)
62	ILLUMINA	ss2094849333	Dec 20, 2016 (150)
63	ILLUMINA	ss2094977485	Dec 20, 2016 (150)
64	USC_VALOUEV	ss2148001864	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2624496197	Nov 08, 2017 (151)
66	ILLUMINA	ss2632576989	Nov 08, 2017 (151)
67	GRF	ss2697974590	Nov 08, 2017 (151)
68	GNOMAD	ss2761406900	Nov 08, 2017 (151)
69	SWEGEN	ss2987764273	Nov 08, 2017 (151)
70	BIOINF_KMB_FNS_UNIBA	ss3023745291	Nov 08, 2017 (151)
71	CSHL	ss3343713104	Nov 08, 2017 (151)
72	ILLUMINA	ss3626210414	Oct 11, 2018 (152)
73	ILLUMINA	ss3630609829	Oct 11, 2018 (152)
74	ILLUMINA	ss3632910281	Oct 11, 2018 (152)
75	ILLUMINA	ss3633605637	Oct 11, 2018 (152)
76	ILLUMINA	ss3634350599	Oct 11, 2018 (152)
77	ILLUMINA	ss3635299078	Oct 11, 2018 (152)
78	ILLUMINA	ss3636029908	Oct 11, 2018 (152)
79	ILLUMINA	ss3637049570	Oct 11, 2018 (152)
80	ILLUMINA	ss3637787956	Oct 11, 2018 (152)
81	ILLUMINA	ss3640057953	Oct 11, 2018 (152)
82	ILLUMINA	ss3642797193	Oct 11, 2018 (152)
83	URBANLAB	ss3646792567	Oct 11, 2018 (152)
84	ILLUMINA	ss3651472338	Oct 11, 2018 (152)
85	ILLUMINA	ss3651472339	Oct 11, 2018 (152)
86	EVA_DECODE	ss3687796878	Jul 12, 2019 (153)
87	ACPOP	ss3727490961	Jul 12, 2019 (153)
88	ILLUMINA	ss3744651500	Jul 12, 2019 (153)
89	EVA	ss3746816256	Jul 12, 2019 (153)
90	ILLUMINA	ss3772152617	Jul 12, 2019 (153)
91	PACBIO	ss3783568272	Jul 12, 2019 (153)
92	PACBIO	ss3789199272	Jul 12, 2019 (153)
93	PACBIO	ss3794071278	Jul 12, 2019 (153)
94	KHV_HUMAN_GENOMES	ss3799816732	Jul 12, 2019 (153)
95	EVA	ss3826427126	Apr 25, 2020 (154)
96	EVA	ss3836608106	Apr 25, 2020 (154)
97	EVA	ss3842017374	Apr 25, 2020 (154)
98	SGDP_PRJ	ss3850020408	Apr 25, 2020 (154)
99	KRGDB	ss3895232587	Apr 25, 2020 (154)
100	KOGIC	ss3945667533	Apr 25, 2020 (154)
101	TOPMED	ss4468580761	Apr 25, 2021 (155)
102	TOMMO_GENOMICS	ss5146521149	Apr 25, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5244318552	Oct 12, 2022 (156)
104	EVA	ss5314651458	Oct 12, 2022 (156)
105	EVA	ss5322097303	Oct 12, 2022 (156)
106	HUGCELL_USP	ss5444908653	Oct 12, 2022 (156)
107	1000G_HIGH_COVERAGE	ss5517659968	Oct 12, 2022 (156)
108	SANFORD_IMAGENETICS	ss5626604915	Oct 12, 2022 (156)
109	TOMMO_GENOMICS	ss5673729978	Oct 12, 2022 (156)
110	EVA	ss5799499020	Oct 12, 2022 (156)
111	YY_MCH	ss5801265700	Oct 12, 2022 (156)
112	EVA	ss5832674686	Oct 12, 2022 (156)
113	EVA	ss5849110835	Oct 12, 2022 (156)
114	EVA	ss5910273595	Oct 12, 2022 (156)
115	EVA	ss5938398987	Oct 12, 2022 (156)
116	1000Genomes	NC_000001.10 - 155711651	Oct 11, 2018 (152)
117	1000Genomes_30x	NC_000001.11 - 155741860	Oct 12, 2022 (156)
118	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 155711651	Oct 11, 2018 (152)
119	The Danish reference pan genome	NC_000001.10 - 155711651	Apr 25, 2020 (154)
120	gnomAD - Genomes	NC_000001.11 - 155741860	Apr 25, 2021 (155)
121	Genome of the Netherlands Release 5	NC_000001.10 - 155711651	Apr 25, 2020 (154)
122	HapMap	NC_000001.11 - 155741860	Apr 25, 2020 (154)
123	KOREAN population from KRGDB	NC_000001.10 - 155711651	Apr 25, 2020 (154)
124	Korean Genome Project	NC_000001.11 - 155741860	Apr 25, 2020 (154)
125	Northern Sweden	NC_000001.10 - 155711651	Jul 12, 2019 (153)
126	Qatari	NC_000001.10 - 155711651	Apr 25, 2020 (154)
127	SGDP_PRJ	NC_000001.10 - 155711651	Apr 25, 2020 (154)
128	Siberian	NC_000001.10 - 155711651	Apr 25, 2020 (154)
129	8.3KJPN	NC_000001.10 - 155711651	Apr 25, 2021 (155)
130	14KJPN	NC_000001.11 - 155741860	Oct 12, 2022 (156)
131	TopMed	NC_000001.11 - 155741860	Apr 25, 2021 (155)
132	UK 10K study - Twins	NC_000001.10 - 155711651	Oct 11, 2018 (152)
133	A Vietnamese Genetic Variation Database	NC_000001.10 - 155711651	Jul 12, 2019 (153)
134	ALFA	NC_000001.11 - 155741860	Apr 25, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
2409981, ss3895232587	NC_000001.10:155711650:T:A	NC_000001.11:155741859:T:A	(self)
14516268220	NC_000001.11:155741859:T:A	NC_000001.11:155741859:T:A	(self)
ss78154661	NC_000001.8:152524723:T:C	NC_000001.11:155741859:T:C	(self)
ss87826335, ss108603527, ss111163281, ss119034954, ss160796269, ss164133122, ss165230315, ss167139347, ss199093827, ss205068784, ss253512861, ss276053159, ss284153512, ss290638145, ss481311786, ss825677783, ss1585071122, ss1712371401, ss2094849333, ss3642797193	NC_000001.9:153978274:T:C	NC_000001.11:155741859:T:C	(self)
3747477, 2037430, 1710674, 884528, 2409981, 775826, 964937, 2037388, 518218, 4490456, 2037430, 436942, ss218654024, ss230733918, ss238381187, ss481336841, ss482319017, ss485451079, ss537376418, ss554706000, ss648418042, ss778575787, ss783170988, ss784126531, ss832430531, ss834032862, ss975689357, ss1068273582, ss1292954461, ss1425980192, ss1574395305, ss1601228649, ss1644222682, ss1751872976, ss1795100536, ss1918923007, ss1966868565, ss2019976626, ss2094977485, ss2148001864, ss2624496197, ss2632576989, ss2697974590, ss2761406900, ss2987764273, ss3343713104, ss3626210414, ss3630609829, ss3632910281, ss3633605637, ss3634350599, ss3635299078, ss3636029908, ss3637049570, ss3637787956, ss3640057953, ss3651472338, ss3651472339, ss3727490961, ss3744651500, ss3746816256, ss3772152617, ss3783568272, ss3789199272, ss3794071278, ss3826427126, ss3836608106, ss3850020408, ss3895232587, ss5146521149, ss5314651458, ss5322097303, ss5626604915, ss5799499020, ss5832674686, ss5938398987	NC_000001.10:155711650:T:C	NC_000001.11:155741859:T:C	(self)
5185903, 27284895, 177623, 2045534, 7567082, 32187096, 14516268220, ss3023745291, ss3646792567, ss3687796878, ss3799816732, ss3842017374, ss3945667533, ss4468580761, ss5244318552, ss5444908653, ss5517659968, ss5673729978, ss5801265700, ss5849110835, ss5910273595	NC_000001.11:155741859:T:C	NC_000001.11:155741859:T:C	(self)
ss43837850, ss75323586, ss97975260, ss106602395, ss119520070, ss123461915, ss131696237, ss138084293, ss154374245, ss155760240, ss172168445, ss174062908	NT_004487.19:7200292:T:C	NC_000001.11:155741859:T:C	(self)
ss9838527	NT_004668.15:2164051:T:C	NC_000001.11:155741859:T:C	(self)
ss16388853, ss19098844, ss20473269	NT_079484.1:2161482:T:C	NC_000001.11:155741859:T:C	(self)
2409981, ss3895232587	NC_000001.10:155711650:T:G	NC_000001.11:155741859: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 rs6671188

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

rs6671188