Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs16951304

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:67797280 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.223461 (59148/264690, TOPMED)
C=0.211724 (32752/154692, ALFA)
C=0.191220 (26806/140184, GnomAD) (+ 19 more)
T=0.36492 (10312/28258, 14KJPN)
T=0.36915 (6187/16760, 8.3KJPN)
C=0.3034 (1943/6404, 1000G_30x)
C=0.3097 (1551/5008, 1000G)
C=0.1498 (671/4480, Estonian)
C=0.2042 (787/3854, ALSPAC)
C=0.2047 (759/3708, TWINSUK)
T=0.3648 (1069/2930, KOREAN)
C=0.3776 (787/2084, HGDP_Stanford)
C=0.2690 (509/1892, HapMap)
T=0.3614 (662/1832, Korea1K)
C=0.198 (198/998, GoNL)
C=0.162 (97/600, NorthernSweden)
T=0.280 (83/296, SGDP_PRJ)
C=0.412 (89/216, Qatari)
T=0.389 (84/216, Vietnamese)
C=0.13 (10/76, Ancient Sardinia)
C=0.15 (6/40, GENOME_DK)
T=0.35 (7/20, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
MAP2K5 : 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 154786 T=0.788179 C=0.211821
European Sub 135148 T=0.789475 C=0.210525
African Sub 9310 T=0.9171 C=0.0829
African Others Sub 326 T=0.951 C=0.049
African American Sub 8984 T=0.9159 C=0.0841
Asian Sub 630 T=0.375 C=0.625
East Asian Sub 498 T=0.386 C=0.614
Other Asian Sub 132 T=0.333 C=0.667
Latin American 1 Sub 692 T=0.776 C=0.224
Latin American 2 Sub 2264 T=0.4845 C=0.5155
South Asian Sub 184 T=0.647 C=0.353
Other Sub 6558 T=0.7283 C=0.2717


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=0.776539 C=0.223461
Allele Frequency Aggregator Total Global 154692 T=0.788276 C=0.211724
Allele Frequency Aggregator European Sub 135072 T=0.789571 C=0.210429
Allele Frequency Aggregator African Sub 9310 T=0.9171 C=0.0829
Allele Frequency Aggregator Other Sub 6540 T=0.7284 C=0.2716
Allele Frequency Aggregator Latin American 2 Sub 2264 T=0.4845 C=0.5155
Allele Frequency Aggregator Latin American 1 Sub 692 T=0.776 C=0.224
Allele Frequency Aggregator Asian Sub 630 T=0.375 C=0.625
Allele Frequency Aggregator South Asian Sub 184 T=0.647 C=0.353
gnomAD - Genomes Global Study-wide 140184 T=0.808780 C=0.191220
gnomAD - Genomes European Sub 75912 T=0.81025 C=0.18975
gnomAD - Genomes African Sub 42034 T=0.91509 C=0.08491
gnomAD - Genomes American Sub 13640 T=0.60704 C=0.39296
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.6640 C=0.3360
gnomAD - Genomes East Asian Sub 3120 T=0.4090 C=0.5910
gnomAD - Genomes Other Sub 2154 T=0.7623 C=0.2377
14KJPN JAPANESE Study-wide 28258 T=0.36492 C=0.63508
8.3KJPN JAPANESE Study-wide 16760 T=0.36915 C=0.63085
1000Genomes_30x Global Study-wide 6404 T=0.6966 C=0.3034
1000Genomes_30x African Sub 1786 T=0.9356 C=0.0644
1000Genomes_30x Europe Sub 1266 T=0.7828 C=0.2172
1000Genomes_30x South Asian Sub 1202 T=0.6481 C=0.3519
1000Genomes_30x East Asian Sub 1170 T=0.4120 C=0.5880
1000Genomes_30x American Sub 980 T=0.549 C=0.451
1000Genomes Global Study-wide 5008 T=0.6903 C=0.3097
1000Genomes African Sub 1322 T=0.9380 C=0.0620
1000Genomes East Asian Sub 1008 T=0.4077 C=0.5923
1000Genomes Europe Sub 1006 T=0.7803 C=0.2197
1000Genomes South Asian Sub 978 T=0.648 C=0.352
1000Genomes American Sub 694 T=0.558 C=0.442
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.8502 C=0.1498
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.7958 C=0.2042
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.7953 C=0.2047
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.3648 A=0.0000, C=0.6352
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.6224 C=0.3776
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.434 C=0.566
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.662 C=0.338
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.720 C=0.280
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.822 C=0.178
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.979 C=0.021
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.102 C=0.898
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.62 C=0.38
HapMap Global Study-wide 1892 T=0.7310 C=0.2690
HapMap American Sub 770 T=0.664 C=0.336
HapMap African Sub 692 T=0.929 C=0.071
HapMap Asian Sub 254 T=0.386 C=0.614
HapMap Europe Sub 176 T=0.744 C=0.256
Korean Genome Project KOREAN Study-wide 1832 T=0.3614 C=0.6386
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.802 C=0.198
Northern Sweden ACPOP Study-wide 600 T=0.838 C=0.162
SGDP_PRJ Global Study-wide 296 T=0.280 C=0.720
Qatari Global Study-wide 216 T=0.588 C=0.412
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.389 C=0.611
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 76 T=0.87 C=0.13
The Danish reference pan genome Danish Study-wide 40 T=0.85 C=0.15
Siberian Global Study-wide 20 T=0.35 C=0.65
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 15 NC_000015.10:g.67797280T>A
GRCh38.p14 chr 15 NC_000015.10:g.67797280T>C
GRCh37.p13 chr 15 NC_000015.9:g.68089618T>A
GRCh37.p13 chr 15 NC_000015.9:g.68089618T>C
MAP2K5 RefSeqGene NG_029143.1:g.259598T>A
MAP2K5 RefSeqGene NG_029143.1:g.259598T>C
Gene: MAP2K5, mitogen-activated protein kinase kinase 5 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
MAP2K5 transcript variant 3 NM_001206804.2:c.1135-936…

NM_001206804.2:c.1135-9366T>A

N/A Intron Variant
MAP2K5 transcript variant 2 NM_002757.4:c.1213-9366T>A N/A Intron Variant
MAP2K5 transcript variant 1 NM_145160.3:c.1243-9366T>A N/A Intron Variant
MAP2K5 transcript variant X1 XM_011521787.4:c. N/A Genic Downstream Transcript Variant
MAP2K5 transcript variant X2 XM_011521788.4:c. N/A Genic Downstream Transcript Variant
MAP2K5 transcript variant X4 XM_017022414.3:c. N/A Genic Downstream Transcript Variant
MAP2K5 transcript variant X5 XM_047432856.1:c. N/A Genic Downstream Transcript Variant
MAP2K5 transcript variant X3 XR_007064474.1: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 T= A C
GRCh38.p14 chr 15 NC_000015.10:g.67797280= NC_000015.10:g.67797280T>A NC_000015.10:g.67797280T>C
GRCh37.p13 chr 15 NC_000015.9:g.68089618= NC_000015.9:g.68089618T>A NC_000015.9:g.68089618T>C
MAP2K5 RefSeqGene NG_029143.1:g.259598= NG_029143.1:g.259598T>A NG_029143.1:g.259598T>C
MAP2K5 transcript variant 3 NM_001206804.1:c.1135-9366= NM_001206804.1:c.1135-9366T>A NM_001206804.1:c.1135-9366T>C
MAP2K5 transcript variant 3 NM_001206804.2:c.1135-9366= NM_001206804.2:c.1135-9366T>A NM_001206804.2:c.1135-9366T>C
MAP2K5 transcript variant 2 NM_002757.3:c.1213-9366= NM_002757.3:c.1213-9366T>A NM_002757.3:c.1213-9366T>C
MAP2K5 transcript variant 2 NM_002757.4:c.1213-9366= NM_002757.4:c.1213-9366T>A NM_002757.4:c.1213-9366T>C
MAP2K5 transcript variant 1 NM_145160.2:c.1243-9366= NM_145160.2:c.1243-9366T>A NM_145160.2:c.1243-9366T>C
MAP2K5 transcript variant 1 NM_145160.3:c.1243-9366= NM_145160.3:c.1243-9366T>A NM_145160.3:c.1243-9366T>C
MAP2K5 transcript variant X1 XM_005254542.1:c.1213-9366= XM_005254542.1:c.1213-9366T>A XM_005254542.1:c.1213-9366T>C
MAP2K5 transcript variant X2 XM_005254543.1:c.835-9366= XM_005254543.1:c.835-9366T>A XM_005254543.1:c.835-9366T>C
MAP2K5 transcript variant X3 XM_005254544.1:c.763-9366= XM_005254544.1:c.763-9366T>A XM_005254544.1:c.763-9366T>C
MAP2K5 transcript variant X4 XM_005254545.1:c.673-9366= XM_005254545.1:c.673-9366T>A XM_005254545.1:c.673-9366T>C
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#.

101 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 PERLEGEN ss23985966 Sep 20, 2004 (123)
2 ILLUMINA ss67509845 Dec 02, 2006 (127)
3 ILLUMINA ss71201034 May 18, 2007 (127)
4 ILLUMINA ss75364238 Dec 07, 2007 (129)
5 HGSV ss81958295 Dec 16, 2007 (130)
6 BGI ss103248836 Dec 01, 2009 (131)
7 1000GENOMES ss114342888 Jan 25, 2009 (130)
8 KRIBB_YJKIM ss119856530 Dec 01, 2009 (131)
9 GMI ss156684689 Dec 01, 2009 (131)
10 ILLUMINA ss160401709 Dec 01, 2009 (131)
11 COMPLETE_GENOMICS ss168246212 Jul 04, 2010 (132)
12 COMPLETE_GENOMICS ss169808073 Jul 04, 2010 (132)
13 ILLUMINA ss172676305 Jul 04, 2010 (132)
14 1000GENOMES ss226953386 Jul 14, 2010 (132)
15 1000GENOMES ss236822133 Jul 15, 2010 (132)
16 1000GENOMES ss243200815 Jul 15, 2010 (132)
17 GMI ss282302272 May 04, 2012 (137)
18 ILLUMINA ss480118713 May 04, 2012 (137)
19 ILLUMINA ss480127640 May 04, 2012 (137)
20 ILLUMINA ss480823749 Sep 08, 2015 (146)
21 ILLUMINA ss484857270 May 04, 2012 (137)
22 ILLUMINA ss536924168 Sep 08, 2015 (146)
23 TISHKOFF ss564551107 Apr 25, 2013 (138)
24 SSMP ss660285652 Apr 25, 2013 (138)
25 ILLUMINA ss778447951 Sep 08, 2015 (146)
26 ILLUMINA ss782875110 Sep 08, 2015 (146)
27 ILLUMINA ss783839055 Sep 08, 2015 (146)
28 ILLUMINA ss832129325 Sep 08, 2015 (146)
29 ILLUMINA ss833903532 Sep 08, 2015 (146)
30 EVA-GONL ss991908281 Aug 21, 2014 (142)
31 JMKIDD_LAB ss1080217334 Aug 21, 2014 (142)
32 1000GENOMES ss1353939258 Aug 21, 2014 (142)
33 DDI ss1427663045 Apr 01, 2015 (144)
34 EVA_GENOME_DK ss1577684590 Apr 01, 2015 (144)
35 EVA_UK10K_ALSPAC ss1633254453 Apr 01, 2015 (144)
36 EVA_UK10K_TWINSUK ss1676248486 Apr 01, 2015 (144)
37 EVA_DECODE ss1695931905 Apr 01, 2015 (144)
38 EVA_SVP ss1713499278 Apr 01, 2015 (144)
39 ILLUMINA ss1752168964 Sep 08, 2015 (146)
40 WEILL_CORNELL_DGM ss1935313370 Feb 12, 2016 (147)
41 GENOMED ss1968137371 Jul 19, 2016 (147)
42 JJLAB ss2028437703 Sep 14, 2016 (149)
43 USC_VALOUEV ss2156843413 Dec 20, 2016 (150)
44 HUMAN_LONGEVITY ss2207773481 Dec 20, 2016 (150)
45 SYSTEMSBIOZJU ss2628714099 Nov 08, 2017 (151)
46 ILLUMINA ss2633245241 Nov 08, 2017 (151)
47 ILLUMINA ss2635059113 Nov 08, 2017 (151)
48 GRF ss2701320186 Nov 08, 2017 (151)
49 GNOMAD ss2936258849 Nov 08, 2017 (151)
50 AFFY ss2985045212 Nov 08, 2017 (151)
51 AFFY ss2985678907 Nov 08, 2017 (151)
52 SWEGEN ss3013474592 Nov 08, 2017 (151)
53 BIOINF_KMB_FNS_UNIBA ss3028044063 Nov 08, 2017 (151)
54 CSHL ss3351169622 Nov 08, 2017 (151)
55 ILLUMINA ss3627389674 Oct 12, 2018 (152)
56 ILLUMINA ss3631236902 Oct 12, 2018 (152)
57 ILLUMINA ss3633101504 Oct 12, 2018 (152)
58 ILLUMINA ss3633806275 Oct 12, 2018 (152)
59 ILLUMINA ss3634612560 Oct 12, 2018 (152)
60 ILLUMINA ss3635495097 Oct 12, 2018 (152)
61 ILLUMINA ss3636302400 Oct 12, 2018 (152)
62 ILLUMINA ss3637246390 Oct 12, 2018 (152)
63 ILLUMINA ss3638092671 Oct 12, 2018 (152)
64 ILLUMINA ss3640319881 Oct 12, 2018 (152)
65 ILLUMINA ss3643076435 Oct 12, 2018 (152)
66 ILLUMINA ss3653817269 Oct 12, 2018 (152)
67 EGCUT_WGS ss3680621557 Jul 13, 2019 (153)
68 EVA_DECODE ss3698127568 Jul 13, 2019 (153)
69 ACPOP ss3741026925 Jul 13, 2019 (153)
70 ILLUMINA ss3744913084 Jul 13, 2019 (153)
71 EVA ss3753234994 Jul 13, 2019 (153)
72 ILLUMINA ss3772411689 Jul 13, 2019 (153)
73 PACBIO ss3787881513 Jul 13, 2019 (153)
74 PACBIO ss3792888233 Jul 13, 2019 (153)
75 PACBIO ss3797772814 Jul 13, 2019 (153)
76 KHV_HUMAN_GENOMES ss3818546145 Jul 13, 2019 (153)
77 EVA ss3834295962 Apr 27, 2020 (154)
78 EVA ss3840747517 Apr 27, 2020 (154)
79 EVA ss3846236938 Apr 27, 2020 (154)
80 HGDP ss3847527674 Apr 27, 2020 (154)
81 SGDP_PRJ ss3883162630 Apr 27, 2020 (154)
82 KRGDB ss3932365173 Apr 27, 2020 (154)
83 KOGIC ss3976377803 Apr 27, 2020 (154)
84 EVA ss3985724060 Apr 27, 2021 (155)
85 EVA ss4017708097 Apr 27, 2021 (155)
86 TOPMED ss4995557404 Apr 27, 2021 (155)
87 TOMMO_GENOMICS ss5216744265 Apr 27, 2021 (155)
88 1000G_HIGH_COVERAGE ss5298856864 Oct 16, 2022 (156)
89 EVA ss5315793595 Oct 16, 2022 (156)
90 EVA ss5419994473 Oct 16, 2022 (156)
91 HUGCELL_USP ss5492545815 Oct 16, 2022 (156)
92 EVA ss5511470899 Oct 16, 2022 (156)
93 1000G_HIGH_COVERAGE ss5600465763 Oct 16, 2022 (156)
94 SANFORD_IMAGENETICS ss5657745746 Oct 16, 2022 (156)
95 TOMMO_GENOMICS ss5770713200 Oct 16, 2022 (156)
96 EVA ss5799941367 Oct 16, 2022 (156)
97 YY_MCH ss5815439208 Oct 16, 2022 (156)
98 EVA ss5828363706 Oct 16, 2022 (156)
99 EVA ss5851343140 Oct 16, 2022 (156)
100 EVA ss5876357336 Oct 16, 2022 (156)
101 EVA ss5949157910 Oct 16, 2022 (156)
102 1000Genomes NC_000015.9 - 68089618 Oct 12, 2018 (152)
103 1000Genomes_30x NC_000015.10 - 67797280 Oct 16, 2022 (156)
104 The Avon Longitudinal Study of Parents and Children NC_000015.9 - 68089618 Oct 12, 2018 (152)
105 Genetic variation in the Estonian population NC_000015.9 - 68089618 Oct 12, 2018 (152)
106 The Danish reference pan genome NC_000015.9 - 68089618 Apr 27, 2020 (154)
107 gnomAD - Genomes NC_000015.10 - 67797280 Apr 27, 2021 (155)
108 Genome of the Netherlands Release 5 NC_000015.9 - 68089618 Apr 27, 2020 (154)
109 HGDP-CEPH-db Supplement 1 NC_000015.8 - 65876672 Apr 27, 2020 (154)
110 HapMap NC_000015.10 - 67797280 Apr 27, 2020 (154)
111 KOREAN population from KRGDB NC_000015.9 - 68089618 Apr 27, 2020 (154)
112 Korean Genome Project NC_000015.10 - 67797280 Apr 27, 2020 (154)
113 Northern Sweden NC_000015.9 - 68089618 Jul 13, 2019 (153)
114 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000015.9 - 68089618 Apr 27, 2021 (155)
115 Qatari NC_000015.9 - 68089618 Apr 27, 2020 (154)
116 SGDP_PRJ NC_000015.9 - 68089618 Apr 27, 2020 (154)
117 Siberian NC_000015.9 - 68089618 Apr 27, 2020 (154)
118 8.3KJPN NC_000015.9 - 68089618 Apr 27, 2021 (155)
119 14KJPN NC_000015.10 - 67797280 Oct 16, 2022 (156)
120 TopMed NC_000015.10 - 67797280 Apr 27, 2021 (155)
121 UK 10K study - Twins NC_000015.9 - 68089618 Oct 12, 2018 (152)
122 A Vietnamese Genetic Variation Database NC_000015.9 - 68089618 Jul 13, 2019 (153)
123 ALFA NC_000015.10 - 67797280 Apr 27, 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)
rs61102042 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
39542567, ss3932365173 NC_000015.9:68089617:T:A NC_000015.10:67797279:T:A (self)
205566, ss81958295, ss114342888, ss168246212, ss169808073, ss282302272, ss480118713, ss1695931905, ss1713499278, ss2635059113, ss3643076435, ss3847527674 NC_000015.8:65876671:T:C NC_000015.10:67797279:T:C (self)
67028030, 37218820, 26359805, 3906301, 16613305, 39542567, 14311790, 949987, 17355300, 35179610, 9359767, 74713572, 37218820, 8278846, ss226953386, ss236822133, ss243200815, ss480127640, ss480823749, ss484857270, ss536924168, ss564551107, ss660285652, ss778447951, ss782875110, ss783839055, ss832129325, ss833903532, ss991908281, ss1080217334, ss1353939258, ss1427663045, ss1577684590, ss1633254453, ss1676248486, ss1752168964, ss1935313370, ss1968137371, ss2028437703, ss2156843413, ss2628714099, ss2633245241, ss2701320186, ss2936258849, ss2985045212, ss2985678907, ss3013474592, ss3351169622, ss3627389674, ss3631236902, ss3633101504, ss3633806275, ss3634612560, ss3635495097, ss3636302400, ss3637246390, ss3638092671, ss3640319881, ss3653817269, ss3680621557, ss3741026925, ss3744913084, ss3753234994, ss3772411689, ss3787881513, ss3792888233, ss3797772814, ss3834295962, ss3840747517, ss3883162630, ss3932365173, ss3985724060, ss4017708097, ss5216744265, ss5315793595, ss5419994473, ss5511470899, ss5657745746, ss5799941367, ss5828363706, ss5949157910 NC_000015.9:68089617:T:C NC_000015.10:67797279:T:C (self)
87991698, 472543140, 1287035, 32755804, 104550304, 211103064, 7241382588, ss2207773481, ss3028044063, ss3698127568, ss3818546145, ss3846236938, ss3976377803, ss4995557404, ss5298856864, ss5492545815, ss5600465763, ss5770713200, ss5815439208, ss5851343140, ss5876357336 NC_000015.10:67797279:T:C NC_000015.10:67797279:T:C (self)
ss23985966, ss67509845, ss71201034, ss75364238, ss103248836, ss119856530, ss156684689, ss160401709, ss172676305 NT_010194.17:38880174:T:C NC_000015.10:67797279:T:C (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 rs16951304

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