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dbSNP Short Genetic Variations

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.

rs9341767

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:79292733 (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
C>A / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.347890 (92083/264690, TOPMED)
C=0.325974 (74371/228150, ALFA)
C=0.341760 (47832/139958, GnomAD) (+ 19 more)
C=0.34619 (27244/78696, PAGE_STUDY)
C=0.19414 (5486/28258, 14KJPN)
C=0.19547 (3276/16760, 8.3KJPN)
C=0.3164 (2026/6404, 1000G_30x)
C=0.3129 (1567/5008, 1000G)
C=0.2759 (1236/4480, Estonian)
C=0.3308 (1275/3854, ALSPAC)
C=0.3188 (1182/3708, TWINSUK)
C=0.1823 (534/2930, KOREAN)
C=0.1976 (362/1832, Korea1K)
C=0.325 (324/998, GoNL)
C=0.182 (144/790, PRJEB37584)
C=0.310 (186/600, NorthernSweden)
C=0.171 (89/520, SGDP_PRJ)
C=0.351 (115/328, HapMap)
C=0.417 (90/216, Qatari)
C=0.160 (34/212, Vietnamese)
C=0.25 (13/52, Siberian)
C=0.25 (10/40, 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 233186 C=0.326559 T=0.673441
European Sub 204364 C=0.326232 T=0.673768
African Sub 7964 C=0.4426 T=0.5574
African Others Sub 316 C=0.437 T=0.563
African American Sub 7648 C=0.4429 T=0.5571
Asian Sub 3816 C=0.1585 T=0.8415
East Asian Sub 3084 C=0.1719 T=0.8281
Other Asian Sub 732 C=0.102 T=0.898
Latin American 1 Sub 1026 C=0.3548 T=0.6452
Latin American 2 Sub 6584 C=0.2963 T=0.7037
South Asian Sub 366 C=0.303 T=0.697
Other Sub 9066 C=0.3224 T=0.6776


Help

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 C=0.347890 T=0.652110
Allele Frequency Aggregator Total Global 228150 C=0.325974 T=0.674026
Allele Frequency Aggregator European Sub 201270 C=0.326149 T=0.673851
Allele Frequency Aggregator Other Sub 8266 C=0.3229 T=0.6771
Allele Frequency Aggregator African Sub 6822 C=0.4437 T=0.5563
Allele Frequency Aggregator Latin American 2 Sub 6584 C=0.2963 T=0.7037
Allele Frequency Aggregator Asian Sub 3816 C=0.1585 T=0.8415
Allele Frequency Aggregator Latin American 1 Sub 1026 C=0.3548 T=0.6452
Allele Frequency Aggregator South Asian Sub 366 C=0.303 T=0.697
gnomAD - Genomes Global Study-wide 139958 C=0.341760 T=0.658240
gnomAD - Genomes European Sub 75830 C=0.30692 T=0.69308
gnomAD - Genomes African Sub 41908 C=0.42603 T=0.57397
gnomAD - Genomes American Sub 13624 C=0.31929 T=0.68071
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=0.3384 T=0.6616
gnomAD - Genomes East Asian Sub 3128 C=0.1605 T=0.8395
gnomAD - Genomes Other Sub 2146 C=0.3392 T=0.6608
The PAGE Study Global Study-wide 78696 C=0.34619 T=0.65381
The PAGE Study AfricanAmerican Sub 32512 C=0.42963 T=0.57037
The PAGE Study Mexican Sub 10808 C=0.29228 T=0.70772
The PAGE Study Asian Sub 8318 C=0.1759 T=0.8241
The PAGE Study PuertoRican Sub 7918 C=0.3453 T=0.6547
The PAGE Study NativeHawaiian Sub 4534 C=0.2073 T=0.7927
The PAGE Study Cuban Sub 4230 C=0.3530 T=0.6470
The PAGE Study Dominican Sub 3828 C=0.3840 T=0.6160
The PAGE Study CentralAmerican Sub 2450 C=0.3000 T=0.7000
The PAGE Study SouthAmerican Sub 1982 C=0.3224 T=0.6776
The PAGE Study NativeAmerican Sub 1260 C=0.3167 T=0.6833
The PAGE Study SouthAsian Sub 856 C=0.285 T=0.715
14KJPN JAPANESE Study-wide 28258 C=0.19414 T=0.80586
8.3KJPN JAPANESE Study-wide 16760 C=0.19547 T=0.80453
1000Genomes_30x Global Study-wide 6404 C=0.3164 T=0.6836
1000Genomes_30x African Sub 1786 C=0.4306 T=0.5694
1000Genomes_30x Europe Sub 1266 C=0.3144 T=0.6856
1000Genomes_30x South Asian Sub 1202 C=0.3012 T=0.6988
1000Genomes_30x East Asian Sub 1170 C=0.1735 T=0.8265
1000Genomes_30x American Sub 980 C=0.300 T=0.700
1000Genomes Global Study-wide 5008 C=0.3129 T=0.6871
1000Genomes African Sub 1322 C=0.4297 T=0.5703
1000Genomes East Asian Sub 1008 C=0.1716 T=0.8284
1000Genomes Europe Sub 1006 C=0.3121 T=0.6879
1000Genomes South Asian Sub 978 C=0.305 T=0.695
1000Genomes American Sub 694 C=0.308 T=0.692
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.2759 T=0.7241
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.3308 T=0.6692
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.3188 T=0.6812
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.1823 A=0.0000, T=0.8177
Korean Genome Project KOREAN Study-wide 1832 C=0.1976 T=0.8024
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.325 T=0.675
CNV burdens in cranial meningiomas Global Study-wide 790 C=0.182 T=0.818
CNV burdens in cranial meningiomas CRM Sub 790 C=0.182 T=0.818
Northern Sweden ACPOP Study-wide 600 C=0.310 T=0.690
SGDP_PRJ Global Study-wide 520 C=0.171 T=0.829
HapMap Global Study-wide 328 C=0.351 T=0.649
HapMap African Sub 120 C=0.475 T=0.525
HapMap American Sub 118 C=0.339 T=0.661
HapMap Asian Sub 90 C=0.20 T=0.80
Qatari Global Study-wide 216 C=0.417 T=0.583
A Vietnamese Genetic Variation Database Global Study-wide 212 C=0.160 T=0.840
Siberian Global Study-wide 52 C=0.25 T=0.75
The Danish reference pan genome Danish Study-wide 40 C=0.25 T=0.75
Help

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 6 NC_000006.12:g.79292733C>A
GRCh38.p14 chr 6 NC_000006.12:g.79292733C>T
GRCh37.p13 chr 6 NC_000006.11:g.80002450C>A
GRCh37.p13 chr 6 NC_000006.11:g.80002450C>T
Help

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
Help

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 C= A T
GRCh38.p14 chr 6 NC_000006.12:g.79292733= NC_000006.12:g.79292733C>A NC_000006.12:g.79292733C>T
GRCh37.p13 chr 6 NC_000006.11:g.80002450= NC_000006.11:g.80002450C>A NC_000006.11:g.80002450C>T
Help

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#.

113 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_SNP ss12779979 Dec 05, 2003 (119)
2 CSHL-HAPMAP ss17898128 Feb 27, 2004 (120)
3 CSHL-HAPMAP ss19679704 Feb 27, 2004 (120)
4 ABI ss42755944 Mar 15, 2006 (126)
5 PERLEGEN ss68981517 May 16, 2007 (127)
6 BGI ss104329757 Dec 01, 2009 (131)
7 1000GENOMES ss110410012 Jan 24, 2009 (130)
8 1000GENOMES ss114623885 Jan 25, 2009 (130)
9 ILLUMINA-UK ss116565196 Feb 14, 2009 (130)
10 GMI ss157196821 Dec 01, 2009 (131)
11 ILLUMINA ss160978592 Dec 01, 2009 (131)
12 COMPLETE_GENOMICS ss162540363 Jul 04, 2010 (132)
13 COMPLETE_GENOMICS ss163804071 Jul 04, 2010 (132)
14 BUSHMAN ss202070742 Jul 04, 2010 (132)
15 BCM-HGSC-SUB ss207369923 Jul 04, 2010 (132)
16 1000GENOMES ss222492847 Jul 14, 2010 (132)
17 1000GENOMES ss233551030 Jul 15, 2010 (132)
18 1000GENOMES ss240591761 Jul 15, 2010 (132)
19 BL ss254490847 May 09, 2011 (134)
20 GMI ss278885524 May 04, 2012 (137)
21 PJP ss293645069 May 09, 2011 (134)
22 ILLUMINA ss481872700 May 04, 2012 (137)
23 ILLUMINA ss481905486 May 04, 2012 (137)
24 ILLUMINA ss482864403 Sep 08, 2015 (146)
25 ILLUMINA ss485730546 May 04, 2012 (137)
26 ILLUMINA ss537588665 Sep 08, 2015 (146)
27 TISHKOFF ss559316867 Apr 25, 2013 (138)
28 SSMP ss653280861 Apr 25, 2013 (138)
29 ILLUMINA ss778636132 Sep 08, 2015 (146)
30 ILLUMINA ss783310971 Sep 08, 2015 (146)
31 ILLUMINA ss784263085 Sep 08, 2015 (146)
32 ILLUMINA ss832572421 Sep 08, 2015 (146)
33 ILLUMINA ss834093800 Sep 08, 2015 (146)
34 EVA-GONL ss983138656 Aug 21, 2014 (142)
35 JMKIDD_LAB ss1073764847 Aug 21, 2014 (142)
36 1000GENOMES ss1320905753 Aug 21, 2014 (142)
37 DDI ss1430793580 Apr 01, 2015 (144)
38 EVA_GENOME_DK ss1581756213 Apr 01, 2015 (144)
39 EVA_DECODE ss1592684344 Apr 01, 2015 (144)
40 EVA_UK10K_ALSPAC ss1615968265 Apr 01, 2015 (144)
41 EVA_UK10K_TWINSUK ss1658962298 Apr 01, 2015 (144)
42 ILLUMINA ss1752648760 Sep 08, 2015 (146)
43 HAMMER_LAB ss1804521815 Sep 08, 2015 (146)
44 WEILL_CORNELL_DGM ss1926397168 Feb 12, 2016 (147)
45 ILLUMINA ss1946183847 Feb 12, 2016 (147)
46 ILLUMINA ss1958927074 Feb 12, 2016 (147)
47 GENOMED ss1970445245 Jul 19, 2016 (147)
48 JJLAB ss2023841104 Sep 14, 2016 (149)
49 USC_VALOUEV ss2152033375 Dec 20, 2016 (150)
50 HUMAN_LONGEVITY ss2285477365 Dec 20, 2016 (150)
51 SYSTEMSBIOZJU ss2626415386 Nov 08, 2017 (151)
52 ILLUMINA ss2634472616 Nov 08, 2017 (151)
53 GRF ss2707647058 Nov 08, 2017 (151)
54 GNOMAD ss2841173479 Nov 08, 2017 (151)
55 SWEGEN ss2999398865 Nov 08, 2017 (151)
56 ILLUMINA ss3022639552 Nov 08, 2017 (151)
57 BIOINF_KMB_FNS_UNIBA ss3025713903 Nov 08, 2017 (151)
58 CSHL ss3347069777 Nov 08, 2017 (151)
59 ILLUMINA ss3625906176 Oct 12, 2018 (152)
60 ILLUMINA ss3629584969 Oct 12, 2018 (152)
61 ILLUMINA ss3632387879 Oct 12, 2018 (152)
62 ILLUMINA ss3633427274 Oct 12, 2018 (152)
63 ILLUMINA ss3634150420 Oct 12, 2018 (152)
64 ILLUMINA ss3635074955 Oct 12, 2018 (152)
65 ILLUMINA ss3635831116 Oct 12, 2018 (152)
66 ILLUMINA ss3636798636 Oct 12, 2018 (152)
67 ILLUMINA ss3637583947 Oct 12, 2018 (152)
68 ILLUMINA ss3640782255 Oct 12, 2018 (152)
69 ILLUMINA ss3641198211 Oct 12, 2018 (152)
70 ILLUMINA ss3641495419 Oct 12, 2018 (152)
71 ILLUMINA ss3644916914 Oct 12, 2018 (152)
72 URBANLAB ss3648396614 Oct 12, 2018 (152)
73 ILLUMINA ss3653157065 Oct 12, 2018 (152)
74 EGCUT_WGS ss3667272261 Jul 13, 2019 (153)
75 EVA_DECODE ss3717598513 Jul 13, 2019 (153)
76 ILLUMINA ss3726359719 Jul 13, 2019 (153)
77 ACPOP ss3733681861 Jul 13, 2019 (153)
78 ILLUMINA ss3744274076 Jul 13, 2019 (153)
79 ILLUMINA ss3745374885 Jul 13, 2019 (153)
80 EVA ss3765253683 Jul 13, 2019 (153)
81 PAGE_CC ss3771303991 Jul 13, 2019 (153)
82 ILLUMINA ss3772868380 Jul 13, 2019 (153)
83 PACBIO ss3785529780 Jul 13, 2019 (153)
84 PACBIO ss3790872602 Jul 13, 2019 (153)
85 PACBIO ss3795751691 Jul 13, 2019 (153)
86 KHV_HUMAN_GENOMES ss3808404058 Jul 13, 2019 (153)
87 EVA ss3830025988 Apr 26, 2020 (154)
88 EVA ss3838494373 Apr 26, 2020 (154)
89 EVA ss3843941790 Apr 26, 2020 (154)
90 SGDP_PRJ ss3864991094 Apr 26, 2020 (154)
91 KRGDB ss3911869692 Apr 26, 2020 (154)
92 KOGIC ss3959420354 Apr 26, 2020 (154)
93 EVA ss3984571747 Apr 26, 2021 (155)
94 EVA ss4017283639 Apr 26, 2021 (155)
95 TOPMED ss4709730274 Apr 26, 2021 (155)
96 TOMMO_GENOMICS ss5178380368 Apr 26, 2021 (155)
97 1000G_HIGH_COVERAGE ss5269139685 Oct 13, 2022 (156)
98 EVA ss5315167907 Oct 13, 2022 (156)
99 HUGCELL_USP ss5466707427 Oct 13, 2022 (156)
100 EVA ss5508578028 Oct 13, 2022 (156)
101 1000G_HIGH_COVERAGE ss5555431619 Oct 13, 2022 (156)
102 SANFORD_IMAGENETICS ss5624633906 Oct 13, 2022 (156)
103 SANFORD_IMAGENETICS ss5640800466 Oct 13, 2022 (156)
104 TOMMO_GENOMICS ss5716816238 Oct 13, 2022 (156)
105 EVA ss5799693551 Oct 13, 2022 (156)
106 YY_MCH ss5807655217 Oct 13, 2022 (156)
107 EVA ss5842523266 Oct 13, 2022 (156)
108 EVA ss5847298047 Oct 13, 2022 (156)
109 EVA ss5855436169 Oct 13, 2022 (156)
110 EVA ss5884576631 Oct 13, 2022 (156)
111 EVA ss5969298112 Oct 13, 2022 (156)
112 EVA ss5979792440 Oct 13, 2022 (156)
113 EVA ss5980378179 Oct 13, 2022 (156)
114 1000Genomes NC_000006.11 - 80002450 Oct 12, 2018 (152)
115 1000Genomes_30x NC_000006.12 - 79292733 Oct 13, 2022 (156)
116 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 80002450 Oct 12, 2018 (152)
117 Genetic variation in the Estonian population NC_000006.11 - 80002450 Oct 12, 2018 (152)
118 The Danish reference pan genome NC_000006.11 - 80002450 Apr 26, 2020 (154)
119 gnomAD - Genomes NC_000006.12 - 79292733 Apr 26, 2021 (155)
120 Genome of the Netherlands Release 5 NC_000006.11 - 80002450 Apr 26, 2020 (154)
121 HapMap NC_000006.12 - 79292733 Apr 26, 2020 (154)
122 KOREAN population from KRGDB NC_000006.11 - 80002450 Apr 26, 2020 (154)
123 Korean Genome Project NC_000006.12 - 79292733 Apr 26, 2020 (154)
124 Northern Sweden NC_000006.11 - 80002450 Jul 13, 2019 (153)
125 The PAGE Study NC_000006.12 - 79292733 Jul 13, 2019 (153)
126 CNV burdens in cranial meningiomas NC_000006.11 - 80002450 Apr 26, 2021 (155)
127 Qatari NC_000006.11 - 80002450 Apr 26, 2020 (154)
128 SGDP_PRJ NC_000006.11 - 80002450 Apr 26, 2020 (154)
129 Siberian NC_000006.11 - 80002450 Apr 26, 2020 (154)
130 8.3KJPN NC_000006.11 - 80002450 Apr 26, 2021 (155)
131 14KJPN NC_000006.12 - 79292733 Oct 13, 2022 (156)
132 TopMed NC_000006.12 - 79292733 Apr 26, 2021 (155)
133 UK 10K study - Twins NC_000006.11 - 80002450 Oct 12, 2018 (152)
134 A Vietnamese Genetic Variation Database NC_000006.11 - 80002450 Jul 13, 2019 (153)
135 ALFA NC_000006.12 - 79292733 Apr 26, 2021 (155)
Help

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
19047086, ss3911869692 NC_000006.11:80002449:C:A NC_000006.12:79292732:C:A (self)
ss110410012, ss114623885, ss116565196, ss162540363, ss163804071, ss202070742, ss207369923, ss254490847, ss278885524, ss293645069, ss481872700, ss1592684344 NC_000006.10:80059168:C:T NC_000006.12:79292732:C:T (self)
32722566, 18227201, 13010509, 7921152, 8122163, 19047086, 6966726, 121156, 8439098, 17008074, 4549729, 36349675, 18227201, 4051302, ss222492847, ss233551030, ss240591761, ss481905486, ss482864403, ss485730546, ss537588665, ss559316867, ss653280861, ss778636132, ss783310971, ss784263085, ss832572421, ss834093800, ss983138656, ss1073764847, ss1320905753, ss1430793580, ss1581756213, ss1615968265, ss1658962298, ss1752648760, ss1804521815, ss1926397168, ss1946183847, ss1958927074, ss1970445245, ss2023841104, ss2152033375, ss2626415386, ss2634472616, ss2707647058, ss2841173479, ss2999398865, ss3022639552, ss3347069777, ss3625906176, ss3629584969, ss3632387879, ss3633427274, ss3634150420, ss3635074955, ss3635831116, ss3636798636, ss3637583947, ss3640782255, ss3641198211, ss3641495419, ss3644916914, ss3653157065, ss3667272261, ss3733681861, ss3744274076, ss3745374885, ss3765253683, ss3772868380, ss3785529780, ss3790872602, ss3795751691, ss3830025988, ss3838494373, ss3864991094, ss3911869692, ss3984571747, ss4017283639, ss5178380368, ss5315167907, ss5508578028, ss5624633906, ss5640800466, ss5799693551, ss5842523266, ss5847298047, ss5969298112, ss5979792440, ss5980378179 NC_000006.11:80002449:C:T NC_000006.12:79292732:C:T (self)
42957554, 230928874, 3173101, 15798355, 525460, 50653342, 547107832, 7384410158, ss2285477365, ss3025713903, ss3648396614, ss3717598513, ss3726359719, ss3771303991, ss3808404058, ss3843941790, ss3959420354, ss4709730274, ss5269139685, ss5466707427, ss5555431619, ss5716816238, ss5807655217, ss5855436169, ss5884576631 NC_000006.12:79292732:C:T NC_000006.12:79292732:C:T (self)
ss12779979, ss17898128, ss19679704 NT_007299.12:17822620:C:T NC_000006.12:79292732:C:T (self)
ss42755944, ss68981517, ss104329757, ss157196821, ss160978592 NT_007299.13:18122283:C:T NC_000006.12:79292732:C:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs9341767

Help

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.

Software version is: 2.0.1.post761+d5e8e07