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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.

rs1008658

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr4:54733270 (GRCh38.p13) 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>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.490676 (129877/264690, TOPMED)
T=0.474971 (66437/139876, GnomAD)
T=0.38537 (31440/81584, ALFA) (+ 18 more)
T=0.29254 (4903/16760, 8.3KJPN)
T=0.4952 (2480/5008, 1000G)
T=0.3326 (1490/4480, Estonian)
T=0.3643 (1404/3854, ALSPAC)
T=0.3557 (1319/3708, TWINSUK)
T=0.3201 (938/2930, KOREAN)
T=0.4059 (841/2072, HGDP_Stanford)
C=0.4830 (911/1886, HapMap)
T=0.3002 (550/1832, Korea1K)
T=0.361 (360/998, GoNL)
T=0.283 (170/600, NorthernSweden)
T=0.358 (191/534, MGP)
T=0.270 (115/426, SGDP_PRJ)
T=0.343 (74/216, Qatari)
T=0.341 (73/214, Vietnamese)
T=0.23 (12/52, Siberian)
T=0.30 (12/40, GENOME_DK)
T=0.38 (10/26, Ancient Sardinia)
Clinical Significance
Reported in ClinVar
Gene : Consequence
KIT : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
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.p13 chr 4 NC_000004.12:g.54733270T>C
GRCh38.p13 chr 4 NC_000004.12:g.54733270T>G
GRCh37.p13 chr 4 NC_000004.11:g.55599436T>C
GRCh37.p13 chr 4 NC_000004.11:g.55599436T>G
KIT RefSeqGene (LRG_307) NG_007456.1:g.80276T>C
KIT RefSeqGene (LRG_307) NG_007456.1:g.80276T>G
Gene: KIT, KIT proto-oncogene, receptor tyrosine kinase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
KIT transcript variant 1 NM_000222.3:c.2484+78T>C N/A Intron Variant
KIT transcript variant 2 NM_001093772.2:c.2472+78T…

NM_001093772.2:c.2472+78T>C

N/A Intron Variant
KIT transcript variant 3 NM_001385284.1:c.2487+78T…

NM_001385284.1:c.2487+78T>C

N/A Intron Variant
KIT transcript variant 4 NM_001385285.1:c.2481+78T…

NM_001385285.1:c.2481+78T>C

N/A Intron Variant
KIT transcript variant 5 NM_001385286.1:c.2469+78T…

NM_001385286.1:c.2469+78T>C

N/A Intron Variant
KIT transcript variant 6 NM_001385288.1:c.2475+78T…

NM_001385288.1:c.2475+78T>C

N/A Intron Variant
KIT transcript variant 7 NM_001385290.1:c.2484+78T…

NM_001385290.1:c.2484+78T>C

N/A Intron Variant
KIT transcript variant 8 NM_001385292.1:c.2472+78T…

NM_001385292.1:c.2472+78T>C

N/A Intron 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.

Allele: C (allele ID: 861307 )
ClinVar Accession Disease Names Clinical Significance
RCV001250970.1 Squamous cell lung carcinoma Uncertain-Significance

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 81584 T=0.38537 C=0.61463
European Sub 67728 T=0.35650 C=0.64350
African Sub 4736 T=0.7424 C=0.2576
African Others Sub 180 T=0.822 C=0.178
African American Sub 4556 T=0.7392 C=0.2608
Asian Sub 202 T=0.302 C=0.698
East Asian Sub 160 T=0.306 C=0.694
Other Asian Sub 42 T=0.29 C=0.71
Latin American 1 Sub 268 T=0.451 C=0.549
Latin American 2 Sub 1316 T=0.4134 C=0.5866
South Asian Sub 4968 T=0.4207 C=0.5793
Other Sub 2366 T=0.4070 C=0.5930


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=0.490676 C=0.509324
gnomAD - Genomes Global Study-wide 139876 T=0.474971 C=0.525029
gnomAD - Genomes European Sub 75788 T=0.34845 C=0.65155
gnomAD - Genomes African Sub 41882 T=0.74082 C=0.25918
gnomAD - Genomes American Sub 13614 T=0.43654 C=0.56346
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.3369 C=0.6631
gnomAD - Genomes East Asian Sub 3122 T=0.3085 C=0.6915
gnomAD - Genomes Other Sub 2146 T=0.4548 C=0.5452
8.3KJPN JAPANESE Study-wide 16760 T=0.29254 C=0.70746
1000Genomes Global Study-wide 5008 T=0.4952 C=0.5048
1000Genomes African Sub 1322 T=0.7965 C=0.2035
1000Genomes East Asian Sub 1008 T=0.3125 C=0.6875
1000Genomes Europe Sub 1006 T=0.3429 C=0.6571
1000Genomes South Asian Sub 978 T=0.479 C=0.521
1000Genomes American Sub 694 T=0.431 C=0.569
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.3326 C=0.6674
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.3643 C=0.6357
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.3557 C=0.6443
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.3201 C=0.6799, G=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2072 T=0.4059 C=0.5941
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.338 C=0.662
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 412 T=0.350 C=0.650
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.269 C=0.731
HGDP-CEPH-db Supplement 1 Europe Sub 310 T=0.377 C=0.623
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.888 C=0.112
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.319 C=0.681
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.60 C=0.40
HapMap Global Study-wide 1886 T=0.5170 C=0.4830
HapMap American Sub 764 T=0.421 C=0.579
HapMap African Sub 692 T=0.749 C=0.251
HapMap Asian Sub 254 T=0.303 C=0.697
HapMap Europe Sub 176 T=0.330 C=0.670
Korean Genome Project KOREAN Study-wide 1832 T=0.3002 C=0.6998
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.361 C=0.639
Northern Sweden ACPOP Study-wide 600 T=0.283 C=0.717
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.358 C=0.642
SGDP_PRJ Global Study-wide 426 T=0.270 C=0.730
Qatari Global Study-wide 216 T=0.343 C=0.657
A Vietnamese Genetic Variation Database Global Study-wide 214 T=0.341 C=0.659
Siberian Global Study-wide 52 T=0.23 C=0.77
The Danish reference pan genome Danish Study-wide 40 T=0.30 C=0.70
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 26 T=0.38 C=0.62
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= C G
GRCh38.p13 chr 4 NC_000004.12:g.54733270= NC_000004.12:g.54733270T>C NC_000004.12:g.54733270T>G
GRCh37.p13 chr 4 NC_000004.11:g.55599436= NC_000004.11:g.55599436T>C NC_000004.11:g.55599436T>G
KIT RefSeqGene (LRG_307) NG_007456.1:g.80276= NG_007456.1:g.80276T>C NG_007456.1:g.80276T>G
KIT transcript variant 1 NM_000222.2:c.2484+78= NM_000222.2:c.2484+78T>C NM_000222.2:c.2484+78T>G
KIT transcript variant 1 NM_000222.3:c.2484+78= NM_000222.3:c.2484+78T>C NM_000222.3:c.2484+78T>G
KIT transcript variant 2 NM_001093772.1:c.2472+78= NM_001093772.1:c.2472+78T>C NM_001093772.1:c.2472+78T>G
KIT transcript variant 2 NM_001093772.2:c.2472+78= NM_001093772.2:c.2472+78T>C NM_001093772.2:c.2472+78T>G
KIT transcript variant 3 NM_001385284.1:c.2487+78= NM_001385284.1:c.2487+78T>C NM_001385284.1:c.2487+78T>G
KIT transcript variant 4 NM_001385285.1:c.2481+78= NM_001385285.1:c.2481+78T>C NM_001385285.1:c.2481+78T>G
KIT transcript variant 5 NM_001385286.1:c.2469+78= NM_001385286.1:c.2469+78T>C NM_001385286.1:c.2469+78T>G
KIT transcript variant 6 NM_001385288.1:c.2475+78= NM_001385288.1:c.2475+78T>C NM_001385288.1:c.2475+78T>G
KIT transcript variant 7 NM_001385290.1:c.2484+78= NM_001385290.1:c.2484+78T>C NM_001385290.1:c.2484+78T>G
KIT transcript variant 8 NM_001385292.1:c.2472+78= NM_001385292.1:c.2472+78T>C NM_001385292.1:c.2472+78T>G
KIT transcript variant X1 XM_005265740.1:c.2487+78= XM_005265740.1:c.2487+78T>C XM_005265740.1:c.2487+78T>G
KIT transcript variant X2 XM_005265741.1:c.2484+78= XM_005265741.1:c.2484+78T>C XM_005265741.1:c.2484+78T>G
KIT transcript variant X3 XM_005265742.1:c.2475+78= XM_005265742.1:c.2475+78T>C XM_005265742.1:c.2475+78T>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#.

112 SubSNP, 21 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1471006 Oct 05, 2000 (86)
2 SC_JCM ss4382859 Mar 26, 2002 (103)
3 PERLEGEN ss24314293 Sep 20, 2004 (123)
4 ABI ss44548638 Mar 14, 2006 (126)
5 ILLUMINA ss65762599 Oct 16, 2006 (127)
6 ILLUMINA ss66696817 Dec 02, 2006 (127)
7 ILLUMINA ss66868575 Dec 02, 2006 (127)
8 ILLUMINA ss66943328 Dec 02, 2006 (127)
9 CSHL-HAPMAP ss68373212 Jan 12, 2007 (127)
10 PERLEGEN ss68899080 May 18, 2007 (127)
11 ILLUMINA ss70358269 May 18, 2007 (127)
12 ILLUMINA ss70464018 May 25, 2008 (130)
13 ILLUMINA ss70985095 May 18, 2007 (127)
14 ILLUMINA ss75630334 Dec 07, 2007 (129)
15 CGM_KYOTO ss76864892 Dec 07, 2007 (129)
16 SI_EXO ss76896261 Dec 07, 2007 (129)
17 HGSV ss83074357 Dec 15, 2007 (130)
18 KRIBB_YJKIM ss83654856 Dec 15, 2007 (130)
19 BCMHGSC_JDW ss92584502 Mar 24, 2008 (129)
20 HUMANGENOME_JCVI ss98959812 Feb 05, 2009 (130)
21 SNP500CANCER ss105437303 Feb 05, 2009 (130)
22 BGI ss105827038 Feb 05, 2009 (130)
23 1000GENOMES ss113065291 Jan 25, 2009 (130)
24 ILLUMINA ss121261524 Dec 01, 2009 (131)
25 ENSEMBL ss134696679 Dec 01, 2009 (131)
26 ENSEMBL ss139613268 Dec 01, 2009 (131)
27 ILLUMINA ss152563717 Dec 01, 2009 (131)
28 GMI ss157260828 Dec 01, 2009 (131)
29 ILLUMINA ss159107957 Dec 01, 2009 (131)
30 COMPLETE_GENOMICS ss162112716 Jul 04, 2010 (132)
31 ILLUMINA ss169249933 Jul 04, 2010 (132)
32 ILLUMINA ss169640887 Jul 04, 2010 (132)
33 BCM-HGSC-SUB ss206273582 Jul 04, 2010 (132)
34 1000GENOMES ss211407326 Jul 14, 2010 (132)
35 1000GENOMES ss220917366 Jul 14, 2010 (132)
36 1000GENOMES ss232386664 Jul 14, 2010 (132)
37 1000GENOMES ss239681102 Jul 15, 2010 (132)
38 BL ss253134996 May 09, 2011 (134)
39 GMI ss277712574 May 04, 2012 (137)
40 GMI ss284906665 Apr 25, 2013 (138)
41 PJP ss293069881 May 09, 2011 (134)
42 ILLUMINA ss483322657 May 04, 2012 (137)
43 ILLUMINA ss484831851 May 04, 2012 (137)
44 ILLUMINA ss535537453 Sep 08, 2015 (146)
45 TISHKOFF ss557506960 Apr 25, 2013 (138)
46 SSMP ss651303314 Apr 25, 2013 (138)
47 ILLUMINA ss780233986 Sep 08, 2015 (146)
48 ILLUMINA ss782104447 Sep 08, 2015 (146)
49 ILLUMINA ss825328000 Jul 19, 2016 (147)
50 ILLUMINA ss832620731 Jul 13, 2019 (153)
51 ILLUMINA ss835719273 Sep 08, 2015 (146)
52 EVA-GONL ss980098215 Aug 21, 2014 (142)
53 JMKIDD_LAB ss1071524781 Aug 21, 2014 (142)
54 1000GENOMES ss1309680841 Aug 21, 2014 (142)
55 DDI ss1429878180 Apr 01, 2015 (144)
56 EVA_GENOME_DK ss1580549157 Apr 01, 2015 (144)
57 EVA_DECODE ss1589595864 Apr 01, 2015 (144)
58 EVA_UK10K_ALSPAC ss1610058182 Apr 01, 2015 (144)
59 EVA_UK10K_TWINSUK ss1653052215 Apr 01, 2015 (144)
60 EVA_MGP ss1711059772 Apr 01, 2015 (144)
61 EVA_SVP ss1712672262 Apr 01, 2015 (144)
62 WEILL_CORNELL_DGM ss1923337342 Feb 12, 2016 (147)
63 GENOMED ss1966658493 Feb 12, 2016 (147)
64 JJLAB ss2022252267 Sep 14, 2016 (149)
65 USC_VALOUEV ss2150377511 Dec 20, 2016 (150)
66 HUMAN_LONGEVITY ss2262838324 Dec 20, 2016 (150)
67 TOPMED ss2430488364 Dec 20, 2016 (150)
68 SYSTEMSBIOZJU ss2625625481 Nov 08, 2017 (151)
69 ILLUMINA ss2634118307 Nov 08, 2017 (151)
70 ILLUMINA ss2635132365 Nov 08, 2017 (151)
71 GRF ss2705842720 Nov 08, 2017 (151)
72 GNOMAD ss2809155207 Nov 08, 2017 (151)
73 SWEGEN ss2994678257 Nov 08, 2017 (151)
74 BIOINF_KMB_FNS_UNIBA ss3024897327 Nov 08, 2017 (151)
75 CSHL ss3345707347 Nov 08, 2017 (151)
76 TOPMED ss3428733777 Nov 08, 2017 (151)
77 ILLUMINA ss3628963563 Oct 12, 2018 (152)
78 ILLUMINA ss3632055102 Oct 12, 2018 (152)
79 ILLUMINA ss3638486269 Oct 12, 2018 (152)
80 ILLUMINA ss3639246132 Oct 12, 2018 (152)
81 ILLUMINA ss3639644006 Oct 12, 2018 (152)
82 ILLUMINA ss3642335096 Oct 12, 2018 (152)
83 ILLUMINA ss3643437684 Oct 12, 2018 (152)
84 OMUKHERJEE_ADBS ss3646307585 Oct 12, 2018 (152)
85 URBANLAB ss3647726096 Oct 12, 2018 (152)
86 EGCUT_WGS ss3662563337 Jul 13, 2019 (153)
87 EVA_DECODE ss3712025727 Jul 13, 2019 (153)
88 ACPOP ss3731135575 Jul 13, 2019 (153)
89 EVA ss3761780685 Jul 13, 2019 (153)
90 PACBIO ss3784710131 Jul 13, 2019 (153)
91 PACBIO ss3790168375 Jul 13, 2019 (153)
92 PACBIO ss3795043486 Jul 13, 2019 (153)
93 KHV_HUMAN_GENOMES ss3804915998 Jul 13, 2019 (153)
94 EVA ss3828531330 Apr 26, 2020 (154)
95 EVA ss3837702928 Apr 26, 2020 (154)
96 EVA ss3843138992 Apr 26, 2020 (154)
97 HGDP ss3847750255 Apr 26, 2020 (154)
98 SGDP_PRJ ss3858917371 Apr 26, 2020 (154)
99 KRGDB ss3905154712 Apr 26, 2020 (154)
100 KOGIC ss3954162748 Apr 26, 2020 (154)
101 FSA-LAB ss3984283433 Apr 26, 2021 (155)
102 FSA-LAB ss3984283434 Apr 26, 2021 (155)
103 EVA ss3985069499 Apr 26, 2021 (155)
104 EVA ss3986280014 Apr 26, 2021 (155)
105 EVA ss4017145699 Apr 26, 2021 (155)
106 TOPMED ss4613414307 Apr 26, 2021 (155)
107 TOMMO_GENOMICS ss5165657093 Apr 26, 2021 (155)
108 CPQ_GEN_INCA ss5236854808 Apr 26, 2021 (155)
109 CPQ_GEN_INCA ss5236860040 Apr 26, 2021 (155)
110 CPQ_GEN_INCA ss5236860041 Apr 26, 2021 (155)
111 CPQ_GEN_INCA ss5236860042 Apr 26, 2021 (155)
112 EVA ss5237182000 Apr 26, 2021 (155)
113 1000Genomes NC_000004.11 - 55599436 Oct 12, 2018 (152)
114 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 55599436 Oct 12, 2018 (152)
115 Genetic variation in the Estonian population NC_000004.11 - 55599436 Oct 12, 2018 (152)
116 The Danish reference pan genome NC_000004.11 - 55599436 Apr 26, 2020 (154)
117 gnomAD - Genomes NC_000004.12 - 54733270 Apr 26, 2021 (155)
118 Genome of the Netherlands Release 5 NC_000004.11 - 55599436 Apr 26, 2020 (154)
119 HGDP-CEPH-db Supplement 1 NC_000004.10 - 55294193 Apr 26, 2020 (154)
120 HapMap NC_000004.12 - 54733270 Apr 26, 2020 (154)
121 KOREAN population from KRGDB NC_000004.11 - 55599436 Apr 26, 2020 (154)
122 Korean Genome Project NC_000004.12 - 54733270 Apr 26, 2020 (154)
123 Medical Genome Project healthy controls from Spanish population NC_000004.11 - 55599436 Apr 26, 2020 (154)
124 Northern Sweden NC_000004.11 - 55599436 Jul 13, 2019 (153)
125 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000004.11 - 55599436 Apr 26, 2021 (155)
126 Qatari NC_000004.11 - 55599436 Apr 26, 2020 (154)
127 SGDP_PRJ NC_000004.11 - 55599436 Apr 26, 2020 (154)
128 Siberian NC_000004.11 - 55599436 Apr 26, 2020 (154)
129 8.3KJPN NC_000004.11 - 55599436 Apr 26, 2021 (155)
130 TopMed NC_000004.12 - 54733270 Apr 26, 2021 (155)
131 UK 10K study - Twins NC_000004.11 - 55599436 Oct 12, 2018 (152)
132 A Vietnamese Genetic Variation Database NC_000004.11 - 55599436 Jul 13, 2019 (153)
133 ALFA NC_000004.12 - 54733270 Apr 26, 2021 (155)
134 ClinVar RCV001250970.1 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)
rs17830212 Oct 07, 2004 (123)
rs59003977 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss83074357, ss3639246132, ss3639644006 NC_000004.9:55440363:T:C NC_000004.12:54733269:T:C (self)
428147, ss92584502, ss113065291, ss162112716, ss206273582, ss211407326, ss253134996, ss277712574, ss284906665, ss293069881, ss484831851, ss825328000, ss1589595864, ss1712672262, ss2635132365, ss3643437684, ss3847750255 NC_000004.10:55294192:T:C NC_000004.12:54733269:T:C (self)
21073969, 11728687, 8301585, 6714096, 5170760, 12332106, 175532, 4420440, 295426, 5379272, 10934351, 2893865, 23626400, 11728687, 2575368, ss220917366, ss232386664, ss239681102, ss483322657, ss535537453, ss557506960, ss651303314, ss780233986, ss782104447, ss832620731, ss835719273, ss980098215, ss1071524781, ss1309680841, ss1429878180, ss1580549157, ss1610058182, ss1653052215, ss1711059772, ss1923337342, ss1966658493, ss2022252267, ss2150377511, ss2430488364, ss2625625481, ss2634118307, ss2705842720, ss2809155207, ss2994678257, ss3345707347, ss3628963563, ss3632055102, ss3638486269, ss3642335096, ss3646307585, ss3662563337, ss3731135575, ss3761780685, ss3784710131, ss3790168375, ss3795043486, ss3828531330, ss3837702928, ss3858917371, ss3905154712, ss3984283433, ss3984283434, ss3985069499, ss3986280014, ss4017145699, ss5165657093, ss5236854808, ss5236860040, ss5236860041, ss5236860042 NC_000004.11:55599435:T:C NC_000004.12:54733269:T:C (self)
RCV001250970.1, 149382082, 2613143, 10540749, 281765838, 450791863, 5173367571, ss2262838324, ss3024897327, ss3428733777, ss3647726096, ss3712025727, ss3804915998, ss3843138992, ss3954162748, ss4613414307, ss5237182000 NC_000004.12:54733269:T:C NC_000004.12:54733269:T:C (self)
ss76896261 NT_022853.14:2939318:T:C NC_000004.12:54733269:T:C (self)
ss1471006, ss4382859, ss24314293, ss44548638, ss65762599, ss66696817, ss66868575, ss66943328, ss68373212, ss68899080, ss70358269, ss70464018, ss70985095, ss75630334, ss76864892, ss83654856, ss98959812, ss105437303, ss105827038, ss121261524, ss134696679, ss139613268, ss152563717, ss157260828, ss159107957, ss169249933, ss169640887 NT_022853.15:2939318:T:C NC_000004.12:54733269:T:C (self)
12332106, ss3905154712 NC_000004.11:55599435:T:G NC_000004.12:54733269: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 rs1008658

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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.

Software version is: 2.0.1.post596+ae089ad