Name: rs6759065
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.

rs6759065

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:134631627 (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: A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.435619 (115304/264690, TOPMED)
A=0.411062 (104316/253772, ALFA)
A=0.414796 (58098/140064, GnomAD) (+ 21 more)
G=0.49500 (38421/77618, PAGE_STUDY)
G=0.24119 (6815/28256, 14KJPN)
G=0.24344 (4080/16760, 8.3KJPN)
G=0.4789 (3067/6404, 1000G_30x)
G=0.4738 (2373/5008, 1000G)
A=0.3781 (1694/4480, Estonian)
A=0.3425 (1320/3854, ALSPAC)
A=0.3287 (1219/3708, TWINSUK)
G=0.2386 (699/2930, KOREAN)
G=0.4060 (846/2084, HGDP_Stanford)
G=0.4783 (905/1892, HapMap)
G=0.2265 (415/1832, Korea1K)
A=0.332 (331/998, GoNL)
G=0.225 (178/792, PRJEB37584)
A=0.258 (155/600, NorthernSweden)
A=0.309 (102/330, SGDP_PRJ)
G=0.301 (65/216, Qatari)
G=0.344 (73/212, Vietnamese)
G=0.20 (18/88, Ancient Sardinia)
A=0.27 (12/44, Siberian)
A=0.30 (12/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TMEM163 : 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	258808	A=0.410779	G=0.589221
European	Sub	230284	A=0.400162	G=0.599838
African	Sub	8748	A=0.4415	G=0.5585
African Others	Sub	342	A=0.485	G=0.515
African American	Sub	8406	A=0.4397	G=0.5603
Asian	Sub	3566	A=0.7608	G=0.2392
East Asian	Sub	2866	A=0.7596	G=0.2404
Other Asian	Sub	700	A=0.766	G=0.234
Latin American 1	Sub	948	A=0.475	G=0.525
Latin American 2	Sub	2412	A=0.4208	G=0.5792
South Asian	Sub	346	A=0.497	G=0.503
Other	Sub	12504	A=0.47585	G=0.52415

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	A=0.435619	G=0.564381
Allele Frequency Aggregator	Total	Global	253772	A=0.411062	G=0.588938
Allele Frequency Aggregator	European	Sub	227190	A=0.400665	G=0.599335
Allele Frequency Aggregator	Other	Sub	11704	A=0.47804	G=0.52196
Allele Frequency Aggregator	African	Sub	7606	A=0.4397	G=0.5603
Allele Frequency Aggregator	Asian	Sub	3566	A=0.7608	G=0.2392
Allele Frequency Aggregator	Latin American 2	Sub	2412	A=0.4208	G=0.5792
Allele Frequency Aggregator	Latin American 1	Sub	948	A=0.475	G=0.525
Allele Frequency Aggregator	South Asian	Sub	346	A=0.497	G=0.503
gnomAD - Genomes	Global	Study-wide	140064	A=0.414796	G=0.585204
gnomAD - Genomes	European	Sub	75882	A=0.36383	G=0.63617
gnomAD - Genomes	African	Sub	41956	A=0.44775	G=0.55225
gnomAD - Genomes	American	Sub	13636	A=0.45827	G=0.54173
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.6397	G=0.3603
gnomAD - Genomes	East Asian	Sub	3122	A=0.7412	G=0.2588
gnomAD - Genomes	Other	Sub	2146	A=0.4734	G=0.5266
The PAGE Study	Global	Study-wide	77618	A=0.50500	G=0.49500
The PAGE Study	AfricanAmerican	Sub	32102	A=0.44471	G=0.55529
The PAGE Study	Mexican	Sub	10676	A=0.43612	G=0.56388
The PAGE Study	Asian	Sub	8200	A=0.7556	G=0.2444
The PAGE Study	PuertoRican	Sub	7804	A=0.4927	G=0.5073
The PAGE Study	NativeHawaiian	Sub	4478	A=0.7032	G=0.2968
The PAGE Study	Cuban	Sub	4158	A=0.5207	G=0.4793
The PAGE Study	Dominican	Sub	3772	A=0.5217	G=0.4783
The PAGE Study	CentralAmerican	Sub	2402	A=0.4546	G=0.5454
The PAGE Study	SouthAmerican	Sub	1948	A=0.4759	G=0.5241
The PAGE Study	NativeAmerican	Sub	1234	A=0.3784	G=0.6216
The PAGE Study	SouthAsian	Sub	844	A=0.540	G=0.460
14KJPN	JAPANESE	Study-wide	28256	A=0.75881	G=0.24119
8.3KJPN	JAPANESE	Study-wide	16760	A=0.75656	G=0.24344
1000Genomes_30x	Global	Study-wide	6404	A=0.5211	G=0.4789
1000Genomes_30x	African	Sub	1786	A=0.4815	G=0.5185
1000Genomes_30x	Europe	Sub	1266	A=0.4084	G=0.5916
1000Genomes_30x	South Asian	Sub	1202	A=0.5349	G=0.4651
1000Genomes_30x	East Asian	Sub	1170	A=0.7410	G=0.2590
1000Genomes_30x	American	Sub	980	A=0.459	G=0.541
1000Genomes	Global	Study-wide	5008	A=0.5262	G=0.4738
1000Genomes	African	Sub	1322	A=0.4728	G=0.5272
1000Genomes	East Asian	Sub	1008	A=0.7341	G=0.2659
1000Genomes	Europe	Sub	1006	A=0.4304	G=0.5696
1000Genomes	South Asian	Sub	978	A=0.526	G=0.474
1000Genomes	American	Sub	694	A=0.465	G=0.535
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.3781	G=0.6219
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.3425	G=0.6575
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.3287	G=0.6713
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.7614	G=0.2386
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.5940	G=0.4060
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.721	G=0.279
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.568	G=0.432
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.700	G=0.300
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.509	G=0.491
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.467	G=0.533
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.403	G=0.597
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.78	G=0.22
HapMap	Global	Study-wide	1892	A=0.5217	G=0.4783
HapMap	American	Sub	770	A=0.506	G=0.494
HapMap	African	Sub	692	A=0.428	G=0.572
HapMap	Asian	Sub	254	A=0.768	G=0.232
HapMap	Europe	Sub	176	A=0.602	G=0.398
Korean Genome Project	KOREAN	Study-wide	1832	A=0.7735	G=0.2265
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.332	G=0.668
CNV burdens in cranial meningiomas	Global	Study-wide	792	A=0.775	G=0.225
CNV burdens in cranial meningiomas	CRM	Sub	792	A=0.775	G=0.225
Northern Sweden	ACPOP	Study-wide	600	A=0.258	G=0.742
SGDP_PRJ	Global	Study-wide	330	A=0.309	G=0.691
Qatari	Global	Study-wide	216	A=0.699	G=0.301
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.656	G=0.344
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	88	A=0.80	G=0.20
Siberian	Global	Study-wide	44	A=0.27	G=0.73
The Danish reference pan genome	Danish	Study-wide	40	A=0.30	G=0.70

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.134631627A>G
GRCh37.p13 chr 2	NC_000002.11:g.135389197A>G

Gene: TMEM163, transmembrane protein 163 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TMEM163 transcript	NM_030923.5:c.323-79536T>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	A=	G
GRCh38.p14 chr 2	NC_000002.12:g.134631627=	NC_000002.12:g.134631627A>G
GRCh37.p13 chr 2	NC_000002.11:g.135389197=	NC_000002.11:g.135389197A>G
TMEM163 transcript	NM_030923.4:c.323-79535=	NM_030923.4:c.323-79535T>C
TMEM163 transcript	NM_030923.5:c.323-79536=	NM_030923.5:c.323-79536T>C
TMEM163 transcript variant X1	XM_005263803.1:c.-11-79535=	XM_005263803.1:c.-11-79535T>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#.

124 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10006309	Jul 11, 2003 (116)
2	WUGSC_SSAHASNP	ss14478607	Dec 05, 2003 (119)
3	CSHL-HAPMAP	ss16826697	Feb 27, 2004 (120)
4	ABI	ss44199045	Mar 15, 2006 (126)
5	ILLUMINA	ss67855293	Dec 01, 2006 (127)
6	ILLUMINA	ss71476427	May 17, 2007 (127)
7	ILLUMINA	ss75368773	Dec 06, 2007 (129)
8	HGSV	ss77767224	Dec 06, 2007 (129)
9	HGSV	ss80962588	Dec 16, 2007 (130)
10	HGSV	ss85858094	Dec 16, 2007 (130)
11	BCMHGSC_JDW	ss91356799	Mar 24, 2008 (129)
12	HUMANGENOME_JCVI	ss97079841	Feb 06, 2009 (130)
13	1000GENOMES	ss109910722	Jan 24, 2009 (130)
14	1000GENOMES	ss110958780	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss117885756	Feb 14, 2009 (130)
16	KRIBB_YJKIM	ss119524593	Dec 01, 2009 (131)
17	ENSEMBL	ss132838870	Dec 01, 2009 (131)
18	ENSEMBL	ss138536533	Dec 01, 2009 (131)
19	GMI	ss157713010	Dec 01, 2009 (131)
20	ILLUMINA	ss160806764	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss164282484	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss165269968	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss167204112	Jul 04, 2010 (132)
24	ILLUMINA	ss174101320	Jul 04, 2010 (132)
25	BUSHMAN	ss201089885	Jul 04, 2010 (132)
26	BCM-HGSC-SUB	ss205795365	Jul 04, 2010 (132)
27	1000GENOMES	ss219525009	Jul 14, 2010 (132)
28	1000GENOMES	ss231372076	Jul 14, 2010 (132)
29	1000GENOMES	ss238878460	Jul 15, 2010 (132)
30	BL	ss253505944	May 09, 2011 (134)
31	GMI	ss276691087	May 04, 2012 (137)
32	GMI	ss284442657	Apr 25, 2013 (138)
33	PJP	ss292373119	May 09, 2011 (134)
34	ILLUMINA	ss481345229	May 04, 2012 (137)
35	ILLUMINA	ss481370793	May 04, 2012 (137)
36	ILLUMINA	ss482350460	Sep 08, 2015 (146)
37	ILLUMINA	ss485467780	May 04, 2012 (137)
38	ILLUMINA	ss537388971	Sep 08, 2015 (146)
39	TISHKOFF	ss555892615	Apr 25, 2013 (138)
40	SSMP	ss649519987	Apr 25, 2013 (138)
41	ILLUMINA	ss778579468	Sep 08, 2015 (146)
42	ILLUMINA	ss783179365	Sep 08, 2015 (146)
43	ILLUMINA	ss784134712	Sep 08, 2015 (146)
44	ILLUMINA	ss832438999	Sep 08, 2015 (146)
45	ILLUMINA	ss834036572	Sep 08, 2015 (146)
46	EVA-GONL	ss977384562	Aug 21, 2014 (142)
47	JMKIDD_LAB	ss1069515171	Aug 21, 2014 (142)
48	1000GENOMES	ss1299429730	Aug 21, 2014 (142)
49	DDI	ss1428748542	Apr 01, 2015 (144)
50	EVA_GENOME_DK	ss1579097126	Apr 01, 2015 (144)
51	EVA_DECODE	ss1586812936	Apr 01, 2015 (144)
52	EVA_UK10K_ALSPAC	ss1604618161	Apr 01, 2015 (144)
53	EVA_UK10K_TWINSUK	ss1647612194	Apr 01, 2015 (144)
54	EVA_SVP	ss1712491880	Apr 01, 2015 (144)
55	ILLUMINA	ss1752312168	Sep 08, 2015 (146)
56	HAMMER_LAB	ss1797570847	Sep 08, 2015 (146)
57	WEILL_CORNELL_DGM	ss1920642818	Feb 12, 2016 (147)
58	ILLUMINA	ss1946052466	Feb 12, 2016 (147)
59	ILLUMINA	ss1958460708	Feb 12, 2016 (147)
60	GENOMED	ss1968894761	Jul 19, 2016 (147)
61	JJLAB	ss2020845480	Sep 14, 2016 (149)
62	CSHL	ss2136678555	Nov 08, 2017 (151)
63	USC_VALOUEV	ss2148911272	Dec 20, 2016 (150)
64	HUMAN_LONGEVITY	ss2234483412	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2624929398	Nov 08, 2017 (151)
66	ILLUMINA	ss2633676095	Nov 08, 2017 (151)
67	GRF	ss2703535526	Nov 08, 2017 (151)
68	ILLUMINA	ss2710912418	Nov 08, 2017 (151)
69	GNOMAD	ss2779950826	Nov 08, 2017 (151)
70	SWEGEN	ss2990470599	Nov 08, 2017 (151)
71	ILLUMINA	ss3022019309	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3024186134	Nov 08, 2017 (151)
73	CSHL	ss3344493484	Nov 08, 2017 (151)
74	ILLUMINA	ss3625765804	Oct 11, 2018 (152)
75	ILLUMINA	ss3628171166	Oct 11, 2018 (152)
76	ILLUMINA	ss3631639570	Oct 11, 2018 (152)
77	ILLUMINA	ss3633217192	Oct 11, 2018 (152)
78	ILLUMINA	ss3633929692	Oct 11, 2018 (152)
79	ILLUMINA	ss3634788497	Oct 11, 2018 (152)
80	ILLUMINA	ss3635615542	Oct 11, 2018 (152)
81	ILLUMINA	ss3636477398	Oct 11, 2018 (152)
82	ILLUMINA	ss3637367485	Oct 11, 2018 (152)
83	ILLUMINA	ss3638288923	Oct 11, 2018 (152)
84	ILLUMINA	ss3640495796	Oct 11, 2018 (152)
85	ILLUMINA	ss3643255745	Oct 11, 2018 (152)
86	ILLUMINA	ss3644755184	Oct 11, 2018 (152)
87	URBANLAB	ss3647150939	Oct 11, 2018 (152)
88	ILLUMINA	ss3652459763	Oct 11, 2018 (152)
89	EGCUT_WGS	ss3658312355	Jul 13, 2019 (153)
90	EVA_DECODE	ss3704941828	Jul 13, 2019 (153)
91	ILLUMINA	ss3725826022	Jul 13, 2019 (153)
92	ACPOP	ss3728889623	Jul 13, 2019 (153)
93	ILLUMINA	ss3744182888	Jul 13, 2019 (153)
94	ILLUMINA	ss3744480106	Jul 13, 2019 (153)
95	ILLUMINA	ss3745088350	Jul 13, 2019 (153)
96	EVA	ss3757412939	Jul 13, 2019 (153)
97	PAGE_CC	ss3770950148	Jul 13, 2019 (153)
98	ILLUMINA	ss3772585027	Jul 13, 2019 (153)
99	KHV_HUMAN_GENOMES	ss3801780593	Jul 13, 2019 (153)
100	EVA	ss3827233855	Apr 25, 2020 (154)
101	EVA	ss3837032500	Apr 25, 2020 (154)
102	EVA	ss3842451108	Apr 25, 2020 (154)
103	HGDP	ss3847633805	Apr 25, 2020 (154)
104	SGDP_PRJ	ss3853468391	Apr 25, 2020 (154)
105	KRGDB	ss3899027793	Apr 25, 2020 (154)
106	KOGIC	ss3949018864	Apr 25, 2020 (154)
107	EVA	ss3984490023	Apr 26, 2021 (155)
108	EVA	ss3984923330	Apr 26, 2021 (155)
109	EVA	ss4017022001	Apr 26, 2021 (155)
110	TOPMED	ss4524808175	Apr 26, 2021 (155)
111	TOMMO_GENOMICS	ss5153981211	Apr 26, 2021 (155)
112	1000G_HIGH_COVERAGE	ss5250104388	Oct 12, 2022 (156)
113	EVA	ss5314770921	Oct 12, 2022 (156)
114	EVA	ss5332503376	Oct 12, 2022 (156)
115	HUGCELL_USP	ss5449908444	Oct 12, 2022 (156)
116	EVA	ss5506597516	Oct 12, 2022 (156)
117	1000G_HIGH_COVERAGE	ss5526419054	Oct 12, 2022 (156)
118	SANFORD_IMAGENETICS	ss5629859709	Oct 12, 2022 (156)
119	TOMMO_GENOMICS	ss5684141043	Oct 12, 2022 (156)
120	YY_MCH	ss5802746072	Oct 12, 2022 (156)
121	EVA	ss5820840886	Oct 12, 2022 (156)
122	EVA	ss5852724746	Oct 12, 2022 (156)
123	EVA	ss5932473384	Oct 12, 2022 (156)
124	EVA	ss5956061831	Oct 12, 2022 (156)
125	1000Genomes	NC_000002.11 - 135389197	Oct 11, 2018 (152)
126	1000Genomes_30x	NC_000002.12 - 134631627	Oct 12, 2022 (156)
127	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 135389197	Oct 11, 2018 (152)
128	Genetic variation in the Estonian population	NC_000002.11 - 135389197	Oct 11, 2018 (152)
129	The Danish reference pan genome	NC_000002.11 - 135389197	Apr 25, 2020 (154)
130	gnomAD - Genomes	NC_000002.12 - 134631627	Apr 26, 2021 (155)
131	Genome of the Netherlands Release 5	NC_000002.11 - 135389197	Apr 25, 2020 (154)
132	HGDP-CEPH-db Supplement 1	NC_000002.10 - 135105667	Apr 25, 2020 (154)
133	HapMap	NC_000002.12 - 134631627	Apr 25, 2020 (154)
134	KOREAN population from KRGDB	NC_000002.11 - 135389197	Apr 25, 2020 (154)
135	Korean Genome Project	NC_000002.12 - 134631627	Apr 25, 2020 (154)
136	Northern Sweden	NC_000002.11 - 135389197	Jul 13, 2019 (153)
137	The PAGE Study	NC_000002.12 - 134631627	Jul 13, 2019 (153)
138	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000002.11 - 135389197	Apr 26, 2021 (155)
139	CNV burdens in cranial meningiomas	NC_000002.11 - 135389197	Apr 26, 2021 (155)
140	Qatari	NC_000002.11 - 135389197	Apr 25, 2020 (154)
141	SGDP_PRJ	NC_000002.11 - 135389197	Apr 25, 2020 (154)
142	Siberian	NC_000002.11 - 135389197	Apr 25, 2020 (154)
143	8.3KJPN	NC_000002.11 - 135389197	Apr 26, 2021 (155)
144	14KJPN	NC_000002.12 - 134631627	Oct 12, 2022 (156)
145	TopMed	NC_000002.12 - 134631627	Apr 26, 2021 (155)
146	UK 10K study - Twins	NC_000002.11 - 135389197	Oct 11, 2018 (152)
147	A Vietnamese Genetic Variation Database	NC_000002.11 - 135389197	Jul 13, 2019 (153)
148	ALFA	NC_000002.12 - 134631627	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)
rs61599980	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77767224, ss80962588, ss85858094	NC_000002.9:135222928:A:G	NC_000002.12:134631626:A:G	(self)
311697, ss91356799, ss109910722, ss110958780, ss117885756, ss164282484, ss165269968, ss167204112, ss201089885, ss205795365, ss253505944, ss276691087, ss284442657, ss292373119, ss481345229, ss1586812936, ss1712491880, ss2136678555, ss3643255745, ss3847633805	NC_000002.10:135105666:A:G	NC_000002.12:134631626:A:G	(self)
10449194, 5755551, 4050603, 5262065, 2530628, 6205187, 2174488, 149257, 39357, 2684748, 5485371, 1427626, 11950518, 5755551, 1245476, ss219525009, ss231372076, ss238878460, ss481370793, ss482350460, ss485467780, ss537388971, ss555892615, ss649519987, ss778579468, ss783179365, ss784134712, ss832438999, ss834036572, ss977384562, ss1069515171, ss1299429730, ss1428748542, ss1579097126, ss1604618161, ss1647612194, ss1752312168, ss1797570847, ss1920642818, ss1946052466, ss1958460708, ss1968894761, ss2020845480, ss2148911272, ss2624929398, ss2633676095, ss2703535526, ss2710912418, ss2779950826, ss2990470599, ss3022019309, ss3344493484, ss3625765804, ss3628171166, ss3631639570, ss3633217192, ss3633929692, ss3634788497, ss3635615542, ss3636477398, ss3637367485, ss3638288923, ss3640495796, ss3644755184, ss3652459763, ss3658312355, ss3728889623, ss3744182888, ss3744480106, ss3745088350, ss3757412939, ss3772585027, ss3827233855, ss3837032500, ss3853468391, ss3899027793, ss3984490023, ss3984923330, ss4017022001, ss5153981211, ss5314770921, ss5332503376, ss5506597516, ss5629859709, ss5820840886, ss5956061831	NC_000002.11:135389196:A:G	NC_000002.12:134631626:A:G	(self)
13944989, 74493867, 1898700, 5396865, 171617, 17978147, 328631054, 5337132925, ss2234483412, ss3024186134, ss3647150939, ss3704941828, ss3725826022, ss3770950148, ss3801780593, ss3842451108, ss3949018864, ss4524808175, ss5250104388, ss5449908444, ss5526419054, ss5684141043, ss5802746072, ss5852724746, ss5932473384	NC_000002.12:134631626:A:G	NC_000002.12:134631626:A:G	(self)
ss10006309	NT_005058.13:3998095:A:G	NC_000002.12:134631626:A:G	(self)
ss14478607, ss16826697	NT_005058.14:3998205:A:G	NC_000002.12:134631626:A:G	(self)
ss44199045, ss67855293, ss71476427, ss75368773, ss97079841, ss119524593, ss132838870, ss138536533, ss157713010, ss160806764, ss174101320	NT_022135.16:25137859:A:G	NC_000002.12:134631626:A: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 rs6759065

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

rs6759065