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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs2342381

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr11:5631743 (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>A
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.121980 (32287/264690, TOPMED)
G=0.122617 (17188/140176, GnomAD)
G=0.00000 (0/28258, 14KJPN) (+ 18 more)
G=0.11868 (2629/22152, ALFA)
G=0.00000 (0/16758, 8.3KJPN)
G=0.1082 (693/6404, 1000G_30x)
G=0.1048 (525/5008, 1000G)
G=0.0902 (404/4480, Estonian)
G=0.1142 (440/3854, ALSPAC)
G=0.1241 (460/3708, TWINSUK)
G=0.0010 (3/2930, KOREAN)
G=0.0005 (1/1832, Korea1K)
G=0.1421 (233/1640, HapMap)
G=0.116 (116/998, GoNL)
G=0.075 (45/600, NorthernSweden)
G=0.070 (38/546, SGDP_PRJ)
G=0.131 (70/534, MGP)
G=0.162 (35/216, Qatari)
G=0.005 (1/216, Vietnamese)
G=0.09 (5/56, Siberian)
G=0.12 (5/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRIM34 : Intron Variant
TRIM5 : Intron Variant
TRIM6-TRIM34 : 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 22152 G=0.11868 A=0.88132
European Sub 15966 G=0.11042 A=0.88958
African Sub 4114 G=0.1619 A=0.8381
African Others Sub 148 G=0.176 A=0.824
African American Sub 3966 G=0.1614 A=0.8386
Asian Sub 124 G=0.008 A=0.992
East Asian Sub 96 G=0.00 A=1.00
Other Asian Sub 28 G=0.04 A=0.96
Latin American 1 Sub 168 G=0.101 A=0.899
Latin American 2 Sub 670 G=0.072 A=0.928
South Asian Sub 98 G=0.13 A=0.87
Other Sub 1012 G=0.1196 A=0.8804


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 G=0.121980 A=0.878020
gnomAD - Genomes Global Study-wide 140176 G=0.122617 A=0.877383
gnomAD - Genomes European Sub 75926 G=0.10920 A=0.89080
gnomAD - Genomes African Sub 42002 G=0.16904 A=0.83096
gnomAD - Genomes American Sub 13644 G=0.07850 A=0.92150
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.1412 A=0.8588
gnomAD - Genomes East Asian Sub 3132 G=0.0022 A=0.9978
gnomAD - Genomes Other Sub 2150 G=0.1163 A=0.8837
14KJPN JAPANESE Study-wide 28258 G=0.00000 A=1.00000
Allele Frequency Aggregator Total Global 22152 G=0.11868 A=0.88132
Allele Frequency Aggregator European Sub 15966 G=0.11042 A=0.88958
Allele Frequency Aggregator African Sub 4114 G=0.1619 A=0.8381
Allele Frequency Aggregator Other Sub 1012 G=0.1196 A=0.8804
Allele Frequency Aggregator Latin American 2 Sub 670 G=0.072 A=0.928
Allele Frequency Aggregator Latin American 1 Sub 168 G=0.101 A=0.899
Allele Frequency Aggregator Asian Sub 124 G=0.008 A=0.992
Allele Frequency Aggregator South Asian Sub 98 G=0.13 A=0.87
8.3KJPN JAPANESE Study-wide 16758 G=0.00000 A=1.00000
1000Genomes_30x Global Study-wide 6404 G=0.1082 A=0.8918
1000Genomes_30x African Sub 1786 G=0.1769 A=0.8231
1000Genomes_30x Europe Sub 1266 G=0.1106 A=0.8894
1000Genomes_30x South Asian Sub 1202 G=0.1323 A=0.8677
1000Genomes_30x East Asian Sub 1170 G=0.0034 A=0.9966
1000Genomes_30x American Sub 980 G=0.076 A=0.924
1000Genomes Global Study-wide 5008 G=0.1048 A=0.8952
1000Genomes African Sub 1322 G=0.1755 A=0.8245
1000Genomes East Asian Sub 1008 G=0.0040 A=0.9960
1000Genomes Europe Sub 1006 G=0.1083 A=0.8917
1000Genomes South Asian Sub 978 G=0.134 A=0.866
1000Genomes American Sub 694 G=0.071 A=0.929
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.0902 A=0.9098
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.1142 A=0.8858
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.1241 A=0.8759
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.0010 A=0.9990
Korean Genome Project KOREAN Study-wide 1832 G=0.0005 A=0.9995
HapMap Global Study-wide 1640 G=0.1421 A=0.8579
HapMap African Sub 692 G=0.182 A=0.818
HapMap American Sub 600 G=0.135 A=0.865
HapMap Europe Sub 176 G=0.148 A=0.852
HapMap Asian Sub 172 G=0.000 A=1.000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.116 A=0.884
Northern Sweden ACPOP Study-wide 600 G=0.075 A=0.925
SGDP_PRJ Global Study-wide 546 G=0.070 A=0.930
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.131 A=0.869
Qatari Global Study-wide 216 G=0.162 A=0.838
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.005 A=0.995
Siberian Global Study-wide 56 G=0.09 A=0.91
The Danish reference pan genome Danish Study-wide 40 G=0.12 A=0.88
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 11 NC_000011.10:g.5631743G>A
GRCh37.p13 chr 11 NC_000011.9:g.5652973G>A
Gene: TRIM6-TRIM34, TRIM6-TRIM34 readthrough (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM6-TRIM34 transcript NM_001003819.4:c.986-512G…

NM_001003819.4:c.986-512G>A

 		N/A Intron Variant
Gene: TRIM34, tripartite motif containing 34 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM34 transcript variant 4 NM_001003827.1:c.-77-512G…

NM_001003827.1:c.-77-512G>A

 		N/A Intron Variant
TRIM34 transcript variant 1 NM_021616.6:c.-77-512G>A N/A Intron Variant
TRIM34 transcript variant 3 NM_130390.2:c. N/A Genic Upstream Transcript Variant
Gene: TRIM5, tripartite motif containing 5 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM5 transcript variant alpha NM_033034.3:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant gamma NM_033092.4:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant delta NM_033093.4:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X1 XM_005253183.4:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X2 XM_005253184.4:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X11 XM_006718358.4:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X4 XM_011520426.4:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X3 XM_017018460.3:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X5 XM_017018461.3:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X12 XM_017018463.3:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X8 XM_047427783.1:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X12 XM_047427784.1:c. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X6 XR_001748014.3:n. N/A Intron Variant
TRIM5 transcript variant X9 XR_007062518.1:n. N/A Intron Variant
TRIM5 transcript variant X10 XR_007062519.1:n. N/A Intron Variant
TRIM5 transcript variant X15 XR_007062522.1:n. N/A Intron Variant
TRIM5 transcript variant X7 XR_007062517.1:n. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X13 XR_007062520.1:n. N/A Genic Downstream Transcript Variant
TRIM5 transcript variant X14 XR_007062521.1:n. N/A Genic Downstream Transcript Variant
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 G= A
GRCh38.p14 chr 11 NC_000011.10:g.5631743= NC_000011.10:g.5631743G>A
GRCh37.p13 chr 11 NC_000011.9:g.5652973= NC_000011.9:g.5652973G>A
TRIM6-TRIM34 transcript NM_001003819.3:c.986-512= NM_001003819.3:c.986-512G>A
TRIM6-TRIM34 transcript NM_001003819.4:c.986-512= NM_001003819.4:c.986-512G>A
TRIM34 transcript variant 4 NM_001003827.1:c.-77-512= NM_001003827.1:c.-77-512G>A
TRIM34 transcript variant 1 NM_021616.5:c.-77-512= NM_021616.5:c.-77-512G>A
TRIM34 transcript variant 1 NM_021616.6:c.-77-512= NM_021616.6:c.-77-512G>A
TRIM34 transcript variant X1 XM_005252986.1:c.-77-512= XM_005252986.1:c.-77-512G>A
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#.

93 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss3295895 Sep 28, 2001 (100)
2 WI_SSAHASNP ss6786907 Feb 20, 2003 (111)
3 SC_SNP ss15616118 Feb 27, 2004 (120)
4 CSHL-HAPMAP ss17415598 Feb 27, 2004 (120)
5 CSHL-HAPMAP ss19193890 Feb 27, 2004 (120)
6 SSAHASNP ss20789701 Apr 05, 2004 (121)
7 PERLEGEN ss69307725 May 18, 2007 (127)
8 AFFY ss74845585 Aug 16, 2007 (128)
9 ILLUMINA ss75161854 Dec 07, 2007 (129)
10 HGSV ss77300163 Dec 07, 2007 (129)
11 HGSV ss78800400 Dec 07, 2007 (129)
12 HGSV ss82508869 Dec 16, 2007 (130)
13 HUMANGENOME_JCVI ss97359045 Feb 06, 2009 (130)
14 BGI ss106718293 Feb 06, 2009 (130)
15 1000GENOMES ss109933356 Jan 24, 2009 (130)
16 ILLUMINA-UK ss118474515 Feb 14, 2009 (130)
17 KRIBB_YJKIM ss119431956 Dec 01, 2009 (131)
18 ENSEMBL ss137693473 Dec 01, 2009 (131)
19 GMI ss155866190 Dec 01, 2009 (131)
20 COMPLETE_GENOMICS ss167719119 Jul 04, 2010 (132)
21 COMPLETE_GENOMICS ss168951296 Jul 04, 2010 (132)
22 COMPLETE_GENOMICS ss170369166 Jul 04, 2010 (132)
23 ILLUMINA ss173298583 Jul 04, 2010 (132)
24 BUSHMAN ss202341287 Jul 04, 2010 (132)
25 BCM-HGSC-SUB ss207554148 Jul 04, 2010 (132)
26 1000GENOMES ss225067722 Jul 14, 2010 (132)
27 1000GENOMES ss235428209 Jul 15, 2010 (132)
28 1000GENOMES ss242085783 Jul 15, 2010 (132)
29 BL ss254852259 May 09, 2011 (134)
30 GMI ss280867151 May 04, 2012 (137)
31 GMI ss286307584 Apr 25, 2013 (138)
32 PJP ss291105627 May 09, 2011 (134)
33 CLINSEQ_SNP ss491638526 May 04, 2012 (137)
34 ILLUMINA ss537079786 Sep 08, 2015 (146)
35 TISHKOFF ss562356818 Apr 25, 2013 (138)
36 SSMP ss657712876 Apr 25, 2013 (138)
37 EVA-GONL ss988163552 Aug 21, 2014 (142)
38 JMKIDD_LAB ss1077468217 Aug 21, 2014 (142)
39 1000GENOMES ss1339954355 Aug 21, 2014 (142)
40 DDI ss1426521324 Apr 01, 2015 (144)
41 EVA_GENOME_DK ss1575494940 Apr 01, 2015 (144)
42 EVA_DECODE ss1597839964 Apr 01, 2015 (144)
43 EVA_UK10K_ALSPAC ss1625903338 Apr 01, 2015 (144)
44 EVA_UK10K_TWINSUK ss1668897371 Apr 01, 2015 (144)
45 EVA_MGP ss1711280887 Apr 01, 2015 (144)
46 EVA_SVP ss1713229855 Apr 01, 2015 (144)
47 HAMMER_LAB ss1806673907 Sep 08, 2015 (146)
48 WEILL_CORNELL_DGM ss1931527821 Feb 12, 2016 (147)
49 GENOMED ss1967280425 Jul 19, 2016 (147)
50 JJLAB ss2026504403 Sep 14, 2016 (149)
51 ILLUMINA ss2095019577 Dec 20, 2016 (150)
52 USC_VALOUEV ss2154791262 Dec 20, 2016 (150)
53 HUMAN_LONGEVITY ss2179856477 Dec 20, 2016 (150)
54 SYSTEMSBIOZJU ss2627720954 Nov 08, 2017 (151)
55 GRF ss2699061388 Nov 08, 2017 (151)
56 GNOMAD ss2895879064 Nov 08, 2017 (151)
57 SWEGEN ss3007529667 Nov 08, 2017 (151)
58 BIOINF_KMB_FNS_UNIBA ss3027045029 Nov 08, 2017 (151)
59 CSHL ss3349432420 Nov 08, 2017 (151)
60 ILLUMINA ss3626589379 Oct 12, 2018 (152)
61 ILLUMINA ss3637888308 Oct 12, 2018 (152)
62 ILLUMINA ss3642888256 Oct 12, 2018 (152)
63 URBANLAB ss3649522663 Oct 12, 2018 (152)
64 ILLUMINA ss3651664692 Oct 12, 2018 (152)
65 EGCUT_WGS ss3674925803 Jul 13, 2019 (153)
66 EVA_DECODE ss3691134341 Jul 13, 2019 (153)
67 ACPOP ss3737882824 Jul 13, 2019 (153)
68 EVA ss3748891872 Jul 13, 2019 (153)
69 PACBIO ss3786853722 Jul 13, 2019 (153)
70 PACBIO ss3792008889 Jul 13, 2019 (153)
71 PACBIO ss3796890916 Jul 13, 2019 (153)
72 KHV_HUMAN_GENOMES ss3814240900 Jul 13, 2019 (153)
73 EVA ss3825791389 Apr 26, 2020 (154)
74 EVA ss3832454893 Apr 26, 2020 (154)
75 EVA ss3839772398 Apr 26, 2020 (154)
76 EVA ss3845248456 Apr 26, 2020 (154)
77 SGDP_PRJ ss3875561175 Apr 26, 2020 (154)
78 KRGDB ss3923784200 Apr 26, 2020 (154)
79 KOGIC ss3969126807 Apr 26, 2020 (154)
80 EVA ss4017520827 Apr 26, 2021 (155)
81 TOPMED ss4873808985 Apr 26, 2021 (155)
82 TOMMO_GENOMICS ss5200505312 Apr 26, 2021 (155)
83 1000G_HIGH_COVERAGE ss5286263837 Oct 16, 2022 (156)
84 EVA ss5397485008 Oct 16, 2022 (156)
85 HUGCELL_USP ss5481581442 Oct 16, 2022 (156)
86 1000G_HIGH_COVERAGE ss5581314139 Oct 16, 2022 (156)
87 SANFORD_IMAGENETICS ss5650555803 Oct 16, 2022 (156)
88 TOMMO_GENOMICS ss5747209142 Oct 16, 2022 (156)
89 YY_MCH ss5812093185 Oct 16, 2022 (156)
90 EVA ss5836206144 Oct 16, 2022 (156)
91 EVA ss5849840253 Oct 16, 2022 (156)
92 EVA ss5918666924 Oct 16, 2022 (156)
93 EVA ss5941858275 Oct 16, 2022 (156)
94 1000Genomes NC_000011.9 - 5652973 Oct 12, 2018 (152)
95 1000Genomes_30x NC_000011.10 - 5631743 Oct 16, 2022 (156)
96 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 5652973 Oct 12, 2018 (152)
97 Genetic variation in the Estonian population NC_000011.9 - 5652973 Oct 12, 2018 (152)
98 The Danish reference pan genome NC_000011.9 - 5652973 Apr 26, 2020 (154)
99 gnomAD - Genomes NC_000011.10 - 5631743 Apr 26, 2021 (155)
100 Genome of the Netherlands Release 5 NC_000011.9 - 5652973 Apr 26, 2020 (154)
101 HapMap NC_000011.10 - 5631743 Apr 26, 2020 (154)
102 KOREAN population from KRGDB NC_000011.9 - 5652973 Apr 26, 2020 (154)
103 Korean Genome Project NC_000011.10 - 5631743 Apr 26, 2020 (154)
104 Medical Genome Project healthy controls from Spanish population NC_000011.9 - 5652973 Apr 26, 2020 (154)
105 Northern Sweden NC_000011.9 - 5652973 Jul 13, 2019 (153)
106 Qatari NC_000011.9 - 5652973 Apr 26, 2020 (154)
107 SGDP_PRJ NC_000011.9 - 5652973 Apr 26, 2020 (154)
108 Siberian NC_000011.9 - 5652973 Apr 26, 2020 (154)
109 8.3KJPN NC_000011.9 - 5652973 Apr 26, 2021 (155)
110 14KJPN NC_000011.10 - 5631743 Oct 16, 2022 (156)
111 TopMed NC_000011.10 - 5631743 Apr 26, 2021 (155)
112 UK 10K study - Twins NC_000011.9 - 5652973 Oct 12, 2018 (152)
113 A Vietnamese Genetic Variation Database NC_000011.9 - 5652973 Jul 13, 2019 (153)
114 ALFA NC_000011.10 - 5631743 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).

Associated ID History Updated (Build)
rs52808179 Sep 21, 2007 (128)
rs61662977 May 27, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss77300163, ss78800400, ss82508869, ss109933356, ss118474515, ss167719119, ss168951296, ss170369166, ss202341287, ss207554148, ss254852259, ss280867151, ss286307584, ss291105627, ss491638526, ss1597839964, ss1713229855, ss3642888256 NC_000011.8:5609548:G:A NC_000011.10:5631742:G:A (self)
52431490, 29121619, 20664051, 2423827, 12983639, 30961594, 396647, 11167689, 13569751, 27578155, 7307616, 58474619, 29121619, 6463748, ss225067722, ss235428209, ss242085783, ss537079786, ss562356818, ss657712876, ss988163552, ss1077468217, ss1339954355, ss1426521324, ss1575494940, ss1625903338, ss1668897371, ss1711280887, ss1806673907, ss1931527821, ss1967280425, ss2026504403, ss2095019577, ss2154791262, ss2627720954, ss2699061388, ss2895879064, ss3007529667, ss3349432420, ss3626589379, ss3637888308, ss3651664692, ss3674925803, ss3737882824, ss3748891872, ss3786853722, ss3792008889, ss3796890916, ss3825791389, ss3832454893, ss3839772398, ss3875561175, ss3923784200, ss4017520827, ss5200505312, ss5397485008, ss5650555803, ss5836206144, ss5941858275 NC_000011.9:5652972:G:A NC_000011.10:5631742:G:A (self)
68840074, 370209650, 539698, 25504808, 81046246, 89354641, 7858779267, ss2179856477, ss3027045029, ss3649522663, ss3691134341, ss3814240900, ss3845248456, ss3969126807, ss4873808985, ss5286263837, ss5481581442, ss5581314139, ss5747209142, ss5812093185, ss5849840253, ss5918666924 NC_000011.10:5631742:G:A NC_000011.10:5631742:G:A (self)
ss15616118, ss17415598, ss19193890, ss20789701 NT_009237.16:4416912:G:A NC_000011.10:5631742:G:A (self)
ss3295895, ss6786907, ss69307725, ss74845585, ss75161854, ss97359045, ss106718293, ss119431956, ss137693473, ss155866190, ss173298583 NT_009237.18:5592972:G:A NC_000011.10:5631742:G:A (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 rs2342381

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