Name: rs6694145
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.

rs6694145

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:152452349 (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: G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.412426 (109165/264690, TOPMED)
G=0.347991 (71554/205620, ALFA)
G=0.404406 (56557/139852, GnomAD) (+ 19 more)
G=0.42691 (33565/78624, PAGE_STUDY)
G=0.17777 (5023/28256, 14KJPN)
G=0.17900 (3000/16760, 8.3KJPN)
G=0.4022 (2576/6404, 1000G_30x)
G=0.3992 (1999/5008, 1000G)
G=0.2717 (1217/4480, Estonian)
G=0.3425 (1320/3854, ALSPAC)
G=0.3395 (1259/3708, TWINSUK)
G=0.2215 (649/2930, KOREAN)
G=0.4019 (758/1886, HapMap)
G=0.2407 (441/1832, Korea1K)
G=0.370 (369/998, GoNL)
G=0.244 (193/792, PRJEB37584)
G=0.317 (190/600, NorthernSweden)
G=0.198 (96/486, SGDP_PRJ)
G=0.454 (98/216, Qatari)
G=0.369 (79/214, Vietnamese)
G=0.15 (8/52, Siberian)
G=0.35 (14/40, 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	210656	G=0.349508	T=0.650492
European	Sub	181124	G=0.339922	T=0.660078
African	Sub	7402	G=0.5742	T=0.4258
African Others	Sub	276	G=0.616	T=0.384
African American	Sub	7126	G=0.5726	T=0.4274
Asian	Sub	742	G=0.261	T=0.739
East Asian	Sub	578	G=0.254	T=0.746
Other Asian	Sub	164	G=0.287	T=0.713
Latin American 1	Sub	884	G=0.430	T=0.570
Latin American 2	Sub	8258	G=0.3426	T=0.6574
South Asian	Sub	200	G=0.270	T=0.730
Other	Sub	12046	G=0.36120	T=0.63880

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	G=0.412426	T=0.587574
Allele Frequency Aggregator	Total	Global	205620	G=0.347991	T=0.652009
Allele Frequency Aggregator	European	Sub	178030	G=0.339617	T=0.660383
Allele Frequency Aggregator	Other	Sub	11246	G=0.35888	T=0.64112
Allele Frequency Aggregator	Latin American 2	Sub	8258	G=0.3426	T=0.6574
Allele Frequency Aggregator	African	Sub	6260	G=0.5749	T=0.4251
Allele Frequency Aggregator	Latin American 1	Sub	884	G=0.430	T=0.570
Allele Frequency Aggregator	Asian	Sub	742	G=0.261	T=0.739
Allele Frequency Aggregator	South Asian	Sub	200	G=0.270	T=0.730
gnomAD - Genomes	Global	Study-wide	139852	G=0.404406	T=0.595594
gnomAD - Genomes	European	Sub	75746	G=0.32634	T=0.67366
gnomAD - Genomes	African	Sub	41890	G=0.56882	T=0.43118
gnomAD - Genomes	American	Sub	13622	G=0.35876	T=0.64124
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.4458	T=0.5542
gnomAD - Genomes	East Asian	Sub	3120	G=0.2622	T=0.7378
gnomAD - Genomes	Other	Sub	2152	G=0.3829	T=0.6171
The PAGE Study	Global	Study-wide	78624	G=0.42691	T=0.57309
The PAGE Study	AfricanAmerican	Sub	32486	G=0.56292	T=0.43708
The PAGE Study	Mexican	Sub	10790	G=0.32159	T=0.67841
The PAGE Study	Asian	Sub	8312	G=0.2122	T=0.7878
The PAGE Study	PuertoRican	Sub	7910	G=0.4145	T=0.5855
The PAGE Study	NativeHawaiian	Sub	4528	G=0.2085	T=0.7915
The PAGE Study	Cuban	Sub	4228	G=0.3770	T=0.6230
The PAGE Study	Dominican	Sub	3828	G=0.4608	T=0.5392
The PAGE Study	CentralAmerican	Sub	2448	G=0.4130	T=0.5870
The PAGE Study	SouthAmerican	Sub	1980	G=0.3823	T=0.6177
The PAGE Study	NativeAmerican	Sub	1260	G=0.3460	T=0.6540
The PAGE Study	SouthAsian	Sub	854	G=0.303	T=0.697
14KJPN	JAPANESE	Study-wide	28256	G=0.17777	T=0.82223
8.3KJPN	JAPANESE	Study-wide	16760	G=0.17900	T=0.82100
1000Genomes_30x	Global	Study-wide	6404	G=0.4022	T=0.5978
1000Genomes_30x	African	Sub	1786	G=0.6092	T=0.3908
1000Genomes_30x	Europe	Sub	1266	G=0.3381	T=0.6619
1000Genomes_30x	South Asian	Sub	1202	G=0.2912	T=0.7088
1000Genomes_30x	East Asian	Sub	1170	G=0.2692	T=0.7308
1000Genomes_30x	American	Sub	980	G=0.403	T=0.597
1000Genomes	Global	Study-wide	5008	G=0.3992	T=0.6008
1000Genomes	African	Sub	1322	G=0.6112	T=0.3888
1000Genomes	East Asian	Sub	1008	G=0.2688	T=0.7312
1000Genomes	Europe	Sub	1006	G=0.3449	T=0.6551
1000Genomes	South Asian	Sub	978	G=0.293	T=0.707
1000Genomes	American	Sub	694	G=0.412	T=0.588
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.2717	T=0.7283
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.3425	T=0.6575
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.3395	T=0.6605
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.2215	C=0.0000, T=0.7785
HapMap	Global	Study-wide	1886	G=0.4019	T=0.5981
HapMap	American	Sub	764	G=0.334	T=0.666
HapMap	African	Sub	692	G=0.581	T=0.419
HapMap	Asian	Sub	254	G=0.173	T=0.827
HapMap	Europe	Sub	176	G=0.324	T=0.676
Korean Genome Project	KOREAN	Study-wide	1832	G=0.2407	T=0.7593
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.370	T=0.630
CNV burdens in cranial meningiomas	Global	Study-wide	792	G=0.244	T=0.756
CNV burdens in cranial meningiomas	CRM	Sub	792	G=0.244	T=0.756
Northern Sweden	ACPOP	Study-wide	600	G=0.317	T=0.683
SGDP_PRJ	Global	Study-wide	486	G=0.198	T=0.802
Qatari	Global	Study-wide	216	G=0.454	T=0.546
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.369	T=0.631
Siberian	Global	Study-wide	52	G=0.15	T=0.85
The Danish reference pan genome	Danish	Study-wide	40	G=0.35	T=0.65

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.152452349G>C
GRCh38.p14 chr 1	NC_000001.11:g.152452349G>T
GRCh37.p13 chr 1	NC_000001.10:g.152424825G>C
GRCh37.p13 chr 1	NC_000001.10:g.152424825G>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	G=	C	T
GRCh38.p14 chr 1	NC_000001.11:g.152452349=	NC_000001.11:g.152452349G>C	NC_000001.11:g.152452349G>T
GRCh37.p13 chr 1	NC_000001.10:g.152424825=	NC_000001.10:g.152424825G>C	NC_000001.10:g.152424825G>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#.

124 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss9885402	Jul 11, 2003 (116)
2	CSHL-HAPMAP	ss16421766	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss19123733	Feb 27, 2004 (120)
4	ABI	ss41150262	Mar 14, 2006 (126)
5	AFFY	ss66497436	Dec 01, 2006 (127)
6	AFFY	ss76320319	Dec 06, 2007 (129)
7	HGSV	ss77513497	Dec 06, 2007 (129)
8	KRIBB_YJKIM	ss82290637	Dec 15, 2007 (130)
9	HGSV	ss83060559	Dec 14, 2007 (130)
10	BCMHGSC_JDW	ss87819586	Mar 23, 2008 (129)
11	HUMANGENOME_JCVI	ss99249629	Feb 04, 2009 (130)
12	BGI	ss106601105	Feb 04, 2009 (130)
13	1000GENOMES	ss108588654	Jan 23, 2009 (130)
14	1000GENOMES	ss111130311	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss119024718	Feb 15, 2009 (130)
16	ENSEMBL	ss138080829	Dec 01, 2009 (131)
17	ENSEMBL	ss139213928	Dec 01, 2009 (131)
18	GMI	ss155733743	Dec 01, 2009 (131)
19	ILLUMINA	ss160798865	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss164084428	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss165204531	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss167115595	Jul 04, 2010 (132)
23	AFFY	ss173249797	Jul 04, 2010 (132)
24	BUSHMAN	ss199066328	Jul 04, 2010 (132)
25	BCM-HGSC-SUB	ss205106036	Jul 04, 2010 (132)
26	1000GENOMES	ss218643529	Jul 14, 2010 (132)
27	1000GENOMES	ss230727017	Jul 14, 2010 (132)
28	1000GENOMES	ss238375587	Jul 15, 2010 (132)
29	BL	ss253497611	May 09, 2011 (134)
30	GMI	ss276045901	May 04, 2012 (137)
31	GMI	ss284150112	Apr 25, 2013 (138)
32	PJP	ss290634260	May 09, 2011 (134)
33	ILLUMINA	ss481320106	May 04, 2012 (137)
34	ILLUMINA	ss481345255	May 04, 2012 (137)
35	ILLUMINA	ss482326809	Sep 08, 2015 (146)
36	ILLUMINA	ss485455199	May 04, 2012 (137)
37	ILLUMINA	ss537379498	Sep 08, 2015 (146)
38	TISHKOFF	ss554678258	Apr 25, 2013 (138)
39	SSMP	ss648404506	Apr 25, 2013 (138)
40	ILLUMINA	ss778576721	Sep 08, 2015 (146)
41	ILLUMINA	ss783173067	Sep 08, 2015 (146)
42	ILLUMINA	ss784128552	Sep 08, 2015 (146)
43	ILLUMINA	ss832432626	Sep 08, 2015 (146)
44	ILLUMINA	ss834033803	Sep 08, 2015 (146)
45	EVA-GONL	ss975668432	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1068258059	Aug 21, 2014 (142)
47	1000GENOMES	ss1292865465	Aug 21, 2014 (142)
48	DDI	ss1425974581	Apr 01, 2015 (144)
49	EVA_GENOME_DK	ss1574384096	Apr 01, 2015 (144)
50	EVA_DECODE	ss1585049231	Apr 01, 2015 (144)
51	EVA_UK10K_ALSPAC	ss1601182958	Apr 01, 2015 (144)
52	EVA_UK10K_TWINSUK	ss1644176991	Apr 01, 2015 (144)
53	EVA_SVP	ss1712369799	Apr 01, 2015 (144)
54	ILLUMINA	ss1751871082	Sep 08, 2015 (146)
55	HAMMER_LAB	ss1795070761	Sep 08, 2015 (146)
56	WEILL_CORNELL_DGM	ss1918900413	Feb 12, 2016 (147)
57	ILLUMINA	ss1946008877	Feb 12, 2016 (147)
58	ILLUMINA	ss1958315726	Feb 12, 2016 (147)
59	GENOMED	ss1966864585	Jul 19, 2016 (147)
60	JJLAB	ss2019967002	Sep 14, 2016 (149)
61	USC_VALOUEV	ss2147990811	Dec 20, 2016 (150)
62	HUMAN_LONGEVITY	ss2166421342	Dec 20, 2016 (150)
63	SYSTEMSBIOZJU	ss2624491028	Nov 08, 2017 (151)
64	ILLUMINA	ss2632574242	Nov 08, 2017 (151)
65	GRF	ss2697962414	Nov 08, 2017 (151)
66	ILLUMINA	ss2710682450	Nov 08, 2017 (151)
67	GNOMAD	ss2761143000	Nov 08, 2017 (151)
68	SWEGEN	ss2987729312	Nov 08, 2017 (151)
69	ILLUMINA	ss3021134406	Nov 08, 2017 (151)
70	BIOINF_KMB_FNS_UNIBA	ss3023740604	Nov 08, 2017 (151)
71	CSHL	ss3343704656	Nov 08, 2017 (151)
72	ILLUMINA	ss3625549673	Oct 11, 2018 (152)
73	ILLUMINA	ss3626204676	Oct 11, 2018 (152)
74	ILLUMINA	ss3630607233	Oct 11, 2018 (152)
75	ILLUMINA	ss3632909444	Oct 11, 2018 (152)
76	ILLUMINA	ss3633604736	Oct 11, 2018 (152)
77	ILLUMINA	ss3634348854	Oct 11, 2018 (152)
78	ILLUMINA	ss3635298204	Oct 11, 2018 (152)
79	ILLUMINA	ss3636027971	Oct 11, 2018 (152)
80	ILLUMINA	ss3637048692	Oct 11, 2018 (152)
81	ILLUMINA	ss3640056211	Oct 11, 2018 (152)
82	ILLUMINA	ss3644504823	Oct 11, 2018 (152)
83	URBANLAB	ss3646788382	Oct 11, 2018 (152)
84	ILLUMINA	ss3651468008	Oct 11, 2018 (152)
85	EGCUT_WGS	ss3655669186	Jul 12, 2019 (153)
86	EVA_DECODE	ss3687753080	Jul 12, 2019 (153)
87	ILLUMINA	ss3725063756	Jul 12, 2019 (153)
88	ACPOP	ss3727474208	Jul 12, 2019 (153)
89	ILLUMINA	ss3744053783	Jul 12, 2019 (153)
90	ILLUMINA	ss3744352070	Jul 12, 2019 (153)
91	ILLUMINA	ss3744649766	Jul 12, 2019 (153)
92	EVA	ss3746790319	Jul 12, 2019 (153)
93	PAGE_CC	ss3770839617	Jul 12, 2019 (153)
94	ILLUMINA	ss3772150921	Jul 12, 2019 (153)
95	PACBIO	ss3783562462	Jul 12, 2019 (153)
96	PACBIO	ss3789194830	Jul 12, 2019 (153)
97	PACBIO	ss3794066821	Jul 12, 2019 (153)
98	KHV_HUMAN_GENOMES	ss3799792025	Jul 12, 2019 (153)
99	EVA	ss3826417246	Apr 25, 2020 (154)
100	EVA	ss3836603224	Apr 25, 2020 (154)
101	EVA	ss3842012363	Apr 25, 2020 (154)
102	SGDP_PRJ	ss3849975352	Apr 25, 2020 (154)
103	KRGDB	ss3895176716	Apr 25, 2020 (154)
104	KOGIC	ss3945621483	Apr 25, 2020 (154)
105	EVA	ss3984464489	Apr 25, 2021 (155)
106	EVA	ss4016937163	Apr 25, 2021 (155)
107	TOPMED	ss4467775349	Apr 25, 2021 (155)
108	TOMMO_GENOMICS	ss5146412302	Apr 25, 2021 (155)
109	1000G_HIGH_COVERAGE	ss5244240383	Oct 12, 2022 (156)
110	EVA	ss5314649968	Oct 12, 2022 (156)
111	HUGCELL_USP	ss5444840191	Oct 12, 2022 (156)
112	EVA	ss5506025205	Oct 12, 2022 (156)
113	1000G_HIGH_COVERAGE	ss5517542833	Oct 12, 2022 (156)
114	SANFORD_IMAGENETICS	ss5624217686	Oct 12, 2022 (156)
115	SANFORD_IMAGENETICS	ss5626561636	Oct 12, 2022 (156)
116	TOMMO_GENOMICS	ss5673585138	Oct 12, 2022 (156)
117	EVA	ss5799498400	Oct 12, 2022 (156)
118	YY_MCH	ss5801247822	Oct 12, 2022 (156)
119	EVA	ss5832645509	Oct 12, 2022 (156)
120	EVA	ss5847166609	Oct 12, 2022 (156)
121	EVA	ss5849103560	Oct 12, 2022 (156)
122	EVA	ss5910186545	Oct 12, 2022 (156)
123	EVA	ss5938354904	Oct 12, 2022 (156)
124	EVA	ss5979289572	Oct 12, 2022 (156)
125	1000Genomes	NC_000001.10 - 152424825	Oct 11, 2018 (152)
126	1000Genomes_30x	NC_000001.11 - 152452349	Oct 12, 2022 (156)
127	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 152424825	Oct 11, 2018 (152)
128	Genetic variation in the Estonian population	NC_000001.10 - 152424825	Oct 11, 2018 (152)
129	The Danish reference pan genome	NC_000001.10 - 152424825	Apr 25, 2020 (154)
130	gnomAD - Genomes	NC_000001.11 - 152452349	Apr 25, 2021 (155)
131	Genome of the Netherlands Release 5	NC_000001.10 - 152424825	Apr 25, 2020 (154)
132	HapMap	NC_000001.11 - 152452349	Apr 25, 2020 (154)
133	KOREAN population from KRGDB	NC_000001.10 - 152424825	Apr 25, 2020 (154)
134	Korean Genome Project	NC_000001.11 - 152452349	Apr 25, 2020 (154)
135	Northern Sweden	NC_000001.10 - 152424825	Jul 12, 2019 (153)
136	The PAGE Study	NC_000001.11 - 152452349	Jul 12, 2019 (153)
137	CNV burdens in cranial meningiomas	NC_000001.10 - 152424825	Apr 25, 2021 (155)
138	Qatari	NC_000001.10 - 152424825	Apr 25, 2020 (154)
139	SGDP_PRJ	NC_000001.10 - 152424825	Apr 25, 2020 (154)
140	Siberian	NC_000001.10 - 152424825	Apr 25, 2020 (154)
141	8.3KJPN	NC_000001.10 - 152424825	Apr 25, 2021 (155)
142	14KJPN	NC_000001.11 - 152452349	Oct 12, 2022 (156)
143	TopMed	NC_000001.11 - 152452349	Apr 25, 2021 (155)
144	UK 10K study - Twins	NC_000001.10 - 152424825	Oct 11, 2018 (152)
145	A Vietnamese Genetic Variation Database	NC_000001.10 - 152424825	Jul 12, 2019 (153)
146	ALFA	NC_000001.11 - 152452349	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).

Associated ID	History Updated (Build)
rs57567884	May 23, 2008 (130)
rs60290172	Feb 26, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
2354110, ss3895176716	NC_000001.10:152424824:G:C	NC_000001.11:152452348:G:C	(self)
ss77513497, ss83060559	NC_000001.8:149237897:G:T	NC_000001.11:152452348:G:T	(self)
ss87819586, ss108588654, ss111130311, ss119024718, ss164084428, ss165204531, ss167115595, ss199066328, ss205106036, ss253497611, ss276045901, ss284150112, ss290634260, ss481320106, ss1585049231, ss1712369799	NC_000001.9:150691448:G:T	NC_000001.11:152452348:G:T	(self)
3655444, 1987077, 1407434, 1703620, 864701, 2354110, 759073, 13803, 942343, 1992332, 507165, 4381609, 1987077, 427717, ss218643529, ss230727017, ss238375587, ss481345255, ss482326809, ss485455199, ss537379498, ss554678258, ss648404506, ss778576721, ss783173067, ss784128552, ss832432626, ss834033803, ss975668432, ss1068258059, ss1292865465, ss1425974581, ss1574384096, ss1601182958, ss1644176991, ss1751871082, ss1795070761, ss1918900413, ss1946008877, ss1958315726, ss1966864585, ss2019967002, ss2147990811, ss2624491028, ss2632574242, ss2697962414, ss2710682450, ss2761143000, ss2987729312, ss3021134406, ss3343704656, ss3625549673, ss3626204676, ss3630607233, ss3632909444, ss3633604736, ss3634348854, ss3635298204, ss3636027971, ss3637048692, ss3640056211, ss3644504823, ss3651468008, ss3655669186, ss3727474208, ss3744053783, ss3744352070, ss3744649766, ss3746790319, ss3772150921, ss3783562462, ss3789194830, ss3794066821, ss3826417246, ss3836603224, ss3849975352, ss3895176716, ss3984464489, ss4016937163, ss5146412302, ss5314649968, ss5506025205, ss5624217686, ss5626561636, ss5799498400, ss5832645509, ss5847166609, ss5938354904, ss5979289572	NC_000001.10:152424824:G:T	NC_000001.11:152452348:G:T	(self)
5068768, 26610468, 173562, 1999484, 61086, 7422242, 31381684, 5380030263, ss2166421342, ss3023740604, ss3646788382, ss3687753080, ss3725063756, ss3770839617, ss3799792025, ss3842012363, ss3945621483, ss4467775349, ss5244240383, ss5444840191, ss5517542833, ss5673585138, ss5801247822, ss5849103560, ss5910186545	NC_000001.11:152452348:G:T	NC_000001.11:152452348:G:T	(self)
ss41150262, ss66497436, ss76320319, ss82290637, ss99249629, ss106601105, ss138080829, ss139213928, ss155733743, ss160798865, ss173249797	NT_004487.19:3913466:G:T	NC_000001.11:152452348:G:T	(self)
ss9885402	NT_032962.4:2846820:G:T	NC_000001.11:152452348:G:T	(self)
ss16421766, ss19123733	NT_032962.5:2915179:G:T	NC_000001.11:152452348:G: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 rs6694145

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

rs6694145