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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.

rs11739327

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:167290985 (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
G=0.198304 (52489/264690, TOPMED)
G=0.193799 (27138/140032, GnomAD)
G=0.42165 (11915/28258, 14KJPN) (+ 19 more)
G=0.14854 (3817/25696, ALFA)
G=0.42405 (7107/16760, 8.3KJPN)
G=0.2483 (1590/6404, 1000G_30x)
G=0.2486 (1245/5008, 1000G)
G=0.1319 (591/4480, Estonian)
G=0.1201 (463/3854, ALSPAC)
G=0.1141 (423/3708, TWINSUK)
G=0.4222 (1237/2930, KOREAN)
G=0.3002 (568/1892, HapMap)
G=0.4012 (735/1832, Korea1K)
G=0.114 (114/998, GoNL)
G=0.065 (41/626, Chileans)
G=0.125 (75/600, NorthernSweden)
G=0.153 (33/216, Qatari)
G=0.311 (66/212, Vietnamese)
T=0.392 (76/194, SGDP_PRJ)
G=0.07 (3/40, GENOME_DK)
G=0.00 (0/30, Ancient Sardinia)
T=0.42 (10/24, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TENM2 : 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 25696 T=0.85146 G=0.14854
European Sub 17396 T=0.88670 G=0.11330
African Sub 3622 T=0.6295 G=0.3705
African Others Sub 126 T=0.603 G=0.397
African American Sub 3496 T=0.6304 G=0.3696
Asian Sub 160 T=0.681 G=0.319
East Asian Sub 102 T=0.588 G=0.412
Other Asian Sub 58 T=0.84 G=0.16
Latin American 1 Sub 292 T=0.829 G=0.171
Latin American 2 Sub 2770 T=0.9271 G=0.0729
South Asian Sub 110 T=0.873 G=0.127
Other Sub 1346 T=0.8611 G=0.1389


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 T=0.801696 G=0.198304
gnomAD - Genomes Global Study-wide 140032 T=0.806201 G=0.193799
gnomAD - Genomes European Sub 75882 T=0.88184 G=0.11816
gnomAD - Genomes African Sub 41910 T=0.63987 G=0.36013
gnomAD - Genomes American Sub 13654 T=0.90494 G=0.09506
gnomAD - Genomes Ashkenazi Jewish Sub 3318 T=0.9310 G=0.0690
gnomAD - Genomes East Asian Sub 3122 T=0.6156 G=0.3844
gnomAD - Genomes Other Sub 2146 T=0.8360 G=0.1640
14KJPN JAPANESE Study-wide 28258 T=0.57835 G=0.42165
Allele Frequency Aggregator Total Global 25696 T=0.85146 G=0.14854
Allele Frequency Aggregator European Sub 17396 T=0.88670 G=0.11330
Allele Frequency Aggregator African Sub 3622 T=0.6295 G=0.3705
Allele Frequency Aggregator Latin American 2 Sub 2770 T=0.9271 G=0.0729
Allele Frequency Aggregator Other Sub 1346 T=0.8611 G=0.1389
Allele Frequency Aggregator Latin American 1 Sub 292 T=0.829 G=0.171
Allele Frequency Aggregator Asian Sub 160 T=0.681 G=0.319
Allele Frequency Aggregator South Asian Sub 110 T=0.873 G=0.127
8.3KJPN JAPANESE Study-wide 16760 T=0.57595 G=0.42405
1000Genomes_30x Global Study-wide 6404 T=0.7517 G=0.2483
1000Genomes_30x African Sub 1786 T=0.6002 G=0.3998
1000Genomes_30x Europe Sub 1266 T=0.8791 G=0.1209
1000Genomes_30x South Asian Sub 1202 T=0.8453 G=0.1547
1000Genomes_30x East Asian Sub 1170 T=0.6145 G=0.3855
1000Genomes_30x American Sub 980 T=0.912 G=0.088
1000Genomes Global Study-wide 5008 T=0.7514 G=0.2486
1000Genomes African Sub 1322 T=0.5998 G=0.4002
1000Genomes East Asian Sub 1008 T=0.6190 G=0.3810
1000Genomes Europe Sub 1006 T=0.8787 G=0.1213
1000Genomes South Asian Sub 978 T=0.849 G=0.151
1000Genomes American Sub 694 T=0.911 G=0.089
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.8681 G=0.1319
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.8799 G=0.1201
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.8859 G=0.1141
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.5778 A=0.0000, C=0.0000, G=0.4222
HapMap Global Study-wide 1892 T=0.6998 G=0.3002
HapMap American Sub 770 T=0.800 G=0.200
HapMap African Sub 692 T=0.577 G=0.423
HapMap Asian Sub 254 T=0.555 G=0.445
HapMap Europe Sub 176 T=0.955 G=0.045
Korean Genome Project KOREAN Study-wide 1832 T=0.5988 G=0.4012
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.886 G=0.114
Chileans Chilean Study-wide 626 T=0.935 G=0.065
Northern Sweden ACPOP Study-wide 600 T=0.875 G=0.125
Qatari Global Study-wide 216 T=0.847 G=0.153
A Vietnamese Genetic Variation Database Global Study-wide 212 T=0.689 G=0.311
SGDP_PRJ Global Study-wide 194 T=0.392 G=0.608
The Danish reference pan genome Danish Study-wide 40 T=0.93 G=0.07
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 30 T=1.00 G=0.00
Siberian Global Study-wide 24 T=0.42 G=0.58
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 5 NC_000005.10:g.167290985T>A
GRCh38.p14 chr 5 NC_000005.10:g.167290985T>C
GRCh38.p14 chr 5 NC_000005.10:g.167290985T>G
GRCh37.p13 chr 5 NC_000005.9:g.166717990T>A
GRCh37.p13 chr 5 NC_000005.9:g.166717990T>C
GRCh37.p13 chr 5 NC_000005.9:g.166717990T>G
Gene: TENM2, teneurin transmembrane protein 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TENM2 transcript variant 1 NM_001122679.2:c.226+5922…

NM_001122679.2:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant 5 NM_001395460.1:c.226+5922…

NM_001395460.1:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant 2 NM_001080428.3:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant 3 NM_001368145.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant 4 NM_001368146.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X2 XM_005265950.3:c.226+5922…

XM_005265950.3:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant X5 XM_011534604.3:c.226+5922…

XM_011534604.3:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant X1 XM_017009661.2:c.226+5922…

XM_017009661.2:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant X4 XM_017009662.2:c.226+5922…

XM_017009662.2:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant X3 XM_047417418.1:c.226+5922…

XM_047417418.1:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant X7 XM_047417419.1:c.226+5922…

XM_047417419.1:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant X8 XM_047417420.1:c.226+5922…

XM_047417420.1:c.226+5922T>A

 		N/A Intron Variant
TENM2 transcript variant X26 XM_005265952.3:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X6 XM_017009663.3:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X12 XM_017009664.2:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X16 XM_017009665.2:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X22 XM_017009668.2:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X23 XM_017009669.2:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X9 XM_047417421.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X10 XM_047417422.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X11 XM_047417423.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X13 XM_047417424.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X14 XM_047417425.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X15 XM_047417426.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X17 XM_047417427.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X18 XM_047417428.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X19 XM_047417429.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X20 XM_047417430.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X21 XM_047417431.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X24 XM_047417432.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X25 XM_047417433.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X27 XM_047417434.1:c. N/A Genic Upstream Transcript Variant
TENM2 transcript variant X28 XM_047417435.1:c. N/A Genic Upstream 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 T= A C G
GRCh38.p14 chr 5 NC_000005.10:g.167290985= NC_000005.10:g.167290985T>A NC_000005.10:g.167290985T>C NC_000005.10:g.167290985T>G
GRCh37.p13 chr 5 NC_000005.9:g.166717990= NC_000005.9:g.166717990T>A NC_000005.9:g.166717990T>C NC_000005.9:g.166717990T>G
TENM2 transcript variant 1 NM_001122679.1:c.226+5922= NM_001122679.1:c.226+5922T>A NM_001122679.1:c.226+5922T>C NM_001122679.1:c.226+5922T>G
TENM2 transcript variant 1 NM_001122679.2:c.226+5922= NM_001122679.2:c.226+5922T>A NM_001122679.2:c.226+5922T>C NM_001122679.2:c.226+5922T>G
TENM2 transcript variant 5 NM_001395460.1:c.226+5922= NM_001395460.1:c.226+5922T>A NM_001395460.1:c.226+5922T>C NM_001395460.1:c.226+5922T>G
TENM2 transcript variant X1 XM_005265950.1:c.226+5922= XM_005265950.1:c.226+5922T>A XM_005265950.1:c.226+5922T>C XM_005265950.1:c.226+5922T>G
TENM2 transcript variant X2 XM_005265950.3:c.226+5922= XM_005265950.3:c.226+5922T>A XM_005265950.3:c.226+5922T>C XM_005265950.3:c.226+5922T>G
TENM2 transcript variant X5 XM_011534604.3:c.226+5922= XM_011534604.3:c.226+5922T>A XM_011534604.3:c.226+5922T>C XM_011534604.3:c.226+5922T>G
TENM2 transcript variant X1 XM_017009661.2:c.226+5922= XM_017009661.2:c.226+5922T>A XM_017009661.2:c.226+5922T>C XM_017009661.2:c.226+5922T>G
TENM2 transcript variant X4 XM_017009662.2:c.226+5922= XM_017009662.2:c.226+5922T>A XM_017009662.2:c.226+5922T>C XM_017009662.2:c.226+5922T>G
TENM2 transcript variant X3 XM_047417418.1:c.226+5922= XM_047417418.1:c.226+5922T>A XM_047417418.1:c.226+5922T>C XM_047417418.1:c.226+5922T>G
TENM2 transcript variant X7 XM_047417419.1:c.226+5922= XM_047417419.1:c.226+5922T>A XM_047417419.1:c.226+5922T>C XM_047417419.1:c.226+5922T>G
TENM2 transcript variant X8 XM_047417420.1:c.226+5922= XM_047417420.1:c.226+5922T>A XM_047417420.1:c.226+5922T>C XM_047417420.1:c.226+5922T>G
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#.

67 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss17052893 Feb 28, 2004 (120)
2 PERLEGEN ss23441957 Sep 20, 2004 (123)
3 ABI ss44660979 Mar 14, 2006 (126)
4 AFFY ss66433585 Nov 30, 2006 (127)
5 AFFY ss76208581 Dec 07, 2007 (129)
6 HGSV ss82702429 Dec 14, 2007 (130)
7 KRIBB_YJKIM ss82912361 Dec 15, 2007 (130)
8 HGSV ss85393247 Dec 14, 2007 (130)
9 BGI ss105967578 Feb 04, 2009 (130)
10 1000GENOMES ss113621968 Jan 25, 2009 (130)
11 ILLUMINA-UK ss116898127 Feb 14, 2009 (130)
12 COMPLETE_GENOMICS ss162865584 Jul 04, 2010 (132)
13 COMPLETE_GENOMICS ss166175161 Jul 04, 2010 (132)
14 AFFY ss172817019 Jul 04, 2010 (132)
15 BUSHMAN ss201172639 Jul 04, 2010 (132)
16 BCM-HGSC-SUB ss206979943 Jul 04, 2010 (132)
17 1000GENOMES ss222100733 Jul 14, 2010 (132)
18 1000GENOMES ss233245119 Jul 14, 2010 (132)
19 1000GENOMES ss240347582 Jul 15, 2010 (132)
20 GMI ss278575831 May 04, 2012 (137)
21 GMI ss285304336 Apr 25, 2013 (138)
22 PJP ss293515449 May 09, 2011 (134)
23 TISHKOFF ss558870774 Apr 25, 2013 (138)
24 SSMP ss652780231 Apr 25, 2013 (138)
25 EVA-GONL ss982381788 Aug 21, 2014 (142)
26 JMKIDD_LAB ss1073235928 Aug 21, 2014 (142)
27 1000GENOMES ss1318217925 Aug 21, 2014 (142)
28 EVA_GENOME_DK ss1581451289 Apr 01, 2015 (144)
29 EVA_DECODE ss1591923045 Apr 01, 2015 (144)
30 EVA_UK10K_ALSPAC ss1614550246 Apr 01, 2015 (144)
31 EVA_UK10K_TWINSUK ss1657544279 Apr 01, 2015 (144)
32 EVA_SVP ss1712819342 Apr 01, 2015 (144)
33 HAMMER_LAB ss1804188314 Sep 08, 2015 (146)
34 WEILL_CORNELL_DGM ss1925633098 Feb 12, 2016 (147)
35 JJLAB ss2023428920 Sep 14, 2016 (149)
36 USC_VALOUEV ss2151588946 Dec 20, 2016 (150)
37 HUMAN_LONGEVITY ss2280266416 Dec 20, 2016 (150)
38 SYSTEMSBIOZJU ss2626202794 Nov 08, 2017 (151)
39 GRF ss2707163615 Nov 08, 2017 (151)
40 GNOMAD ss2833646023 Nov 08, 2017 (151)
41 SWEGEN ss2998193870 Nov 08, 2017 (151)
42 BIOINF_KMB_FNS_UNIBA ss3025497419 Nov 08, 2017 (151)
43 CSHL ss3346739233 Nov 08, 2017 (151)
44 EGCUT_WGS ss3666128076 Jul 13, 2019 (153)
45 EVA_DECODE ss3716191641 Jul 13, 2019 (153)
46 ACPOP ss3733030677 Jul 13, 2019 (153)
47 EVA ss3764372118 Jul 13, 2019 (153)
48 KHV_HUMAN_GENOMES ss3807537009 Jul 13, 2019 (153)
49 EVA ss3829628811 Apr 26, 2020 (154)
50 SGDP_PRJ ss3863495179 Apr 26, 2020 (154)
51 KRGDB ss3910198904 Apr 26, 2020 (154)
52 KOGIC ss3958116449 Apr 26, 2020 (154)
53 EVA ss3985186100 Apr 26, 2021 (155)
54 TOPMED ss4687479481 Apr 26, 2021 (155)
55 TOMMO_GENOMICS ss5175275693 Apr 26, 2021 (155)
56 1000G_HIGH_COVERAGE ss5266720157 Oct 13, 2022 (156)
57 EVA ss5362586113 Oct 13, 2022 (156)
58 HUGCELL_USP ss5464598178 Oct 13, 2022 (156)
59 EVA ss5508299189 Oct 13, 2022 (156)
60 1000G_HIGH_COVERAGE ss5551828782 Oct 13, 2022 (156)
61 SANFORD_IMAGENETICS ss5639378022 Oct 13, 2022 (156)
62 TOMMO_GENOMICS ss5712679334 Oct 13, 2022 (156)
63 YY_MCH ss5806978775 Oct 13, 2022 (156)
64 EVA ss5835983800 Oct 13, 2022 (156)
65 EVA ss5855119323 Oct 13, 2022 (156)
66 EVA ss5897340969 Oct 13, 2022 (156)
67 EVA ss5967873336 Oct 13, 2022 (156)
68 1000Genomes NC_000005.9 - 166717990 Oct 12, 2018 (152)
69 1000Genomes_30x NC_000005.10 - 167290985 Oct 13, 2022 (156)
70 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 166717990 Oct 12, 2018 (152)
71 Chileans NC_000005.9 - 166717990 Apr 26, 2020 (154)
72 Genetic variation in the Estonian population NC_000005.9 - 166717990 Oct 12, 2018 (152)
73 The Danish reference pan genome NC_000005.9 - 166717990 Apr 26, 2020 (154)
74 gnomAD - Genomes NC_000005.10 - 167290985 Apr 26, 2021 (155)
75 Genome of the Netherlands Release 5 NC_000005.9 - 166717990 Apr 26, 2020 (154)
76 HapMap NC_000005.10 - 167290985 Apr 26, 2020 (154)
77 KOREAN population from KRGDB NC_000005.9 - 166717990 Apr 26, 2020 (154)
78 Korean Genome Project NC_000005.10 - 167290985 Apr 26, 2020 (154)
79 Northern Sweden NC_000005.9 - 166717990 Jul 13, 2019 (153)
80 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 166717990 Apr 26, 2021 (155)
81 Qatari NC_000005.9 - 166717990 Apr 26, 2020 (154)
82 SGDP_PRJ NC_000005.9 - 166717990 Apr 26, 2020 (154)
83 Siberian NC_000005.9 - 166717990 Apr 26, 2020 (154)
84 8.3KJPN NC_000005.9 - 166717990 Apr 26, 2021 (155)
85 14KJPN NC_000005.10 - 167290985 Oct 13, 2022 (156)
86 TopMed NC_000005.10 - 167290985 Apr 26, 2021 (155)
87 UK 10K study - Twins NC_000005.9 - 166717990 Oct 12, 2018 (152)
88 A Vietnamese Genetic Variation Database NC_000005.9 - 166717990 Jul 13, 2019 (153)
89 ALFA NC_000005.10 - 167290985 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)
rs57158611 May 23, 2008 (130)
rs59552816 Feb 26, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
17376298, ss3910198904 NC_000005.9:166717989:T:A NC_000005.10:167290984:T:A (self)
17376298, ss3910198904 NC_000005.9:166717989:T:C NC_000005.10:167290984:T:C (self)
ss82702429, ss85393247, ss113621968, ss116898127, ss162865584, ss166175161, ss201172639, ss206979943, ss278575831, ss285304336, ss293515449, ss1591923045, ss1712819342 NC_000005.8:166650567:T:G NC_000005.10:167290984:T:G (self)
29932081, 16660673, 365411, 11866324, 7616228, 7394653, 17376298, 6315542, 412027, 7675028, 15512159, 4105300, 33245000, 16660673, 3692206, ss222100733, ss233245119, ss240347582, ss558870774, ss652780231, ss982381788, ss1073235928, ss1318217925, ss1581451289, ss1614550246, ss1657544279, ss1804188314, ss1925633098, ss2023428920, ss2151588946, ss2626202794, ss2707163615, ss2833646023, ss2998193870, ss3346739233, ss3666128076, ss3733030677, ss3764372118, ss3829628811, ss3863495179, ss3910198904, ss3985186100, ss5175275693, ss5362586113, ss5508299189, ss5639378022, ss5835983800, ss5967873336 NC_000005.9:166717989:T:G NC_000005.10:167290984:T:G (self)
39354717, 211720397, 3020443, 14494450, 46516438, 524857038, 1438727548, ss2280266416, ss3025497419, ss3716191641, ss3807537009, ss3958116449, ss4687479481, ss5266720157, ss5464598178, ss5551828782, ss5712679334, ss5806978775, ss5855119323, ss5897340969 NC_000005.10:167290984:T:G NC_000005.10:167290984:T:G (self)
ss17052893 NT_023133.11:11527547:T:G NC_000005.10:167290984:T:G (self)
ss23441957, ss44660979, ss66433585, ss76208581, ss82912361, ss105967578, ss172817019 NT_023133.13:11529262:T:G NC_000005.10:167290984:T:G (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 rs11739327

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