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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.

rs17843023

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:40960351 (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>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.033673 (8913/264690, TOPMED)
T=0.020628 (5184/251314, GnomAD_exome)
T=0.015797 (3226/204220, ALFA) (+ 26 more)
T=0.030883 (4330/140206, GnomAD)
T=0.020617 (2503/121404, ExAC)
T=0.04823 (3796/78700, PAGE_STUDY)
T=0.04073 (1151/28258, 14KJPN)
T=0.04147 (695/16760, 8.3KJPN)
T=0.03016 (392/12998, GO-ESP)
T=0.0483 (309/6404, 1000G_30x)
T=0.0461 (231/5008, 1000G)
T=0.0078 (35/4480, Estonian)
T=0.0125 (48/3854, ALSPAC)
T=0.0089 (33/3708, TWINSUK)
T=0.0720 (211/2930, KOREAN)
T=0.0576 (109/1892, HapMap)
T=0.0097 (11/1136, Daghestan)
T=0.004 (4/998, GoNL)
T=0.087 (69/792, PRJEB37584)
T=0.006 (4/626, Chileans)
T=0.092 (56/612, Vietnamese)
T=0.002 (1/600, NorthernSweden)
T=0.013 (7/534, MGP)
T=0.007 (2/304, FINRISK)
T=0.009 (2/216, Qatari)
G=0.50 (17/34, SGDP_PRJ)
T=0.50 (17/34, SGDP_PRJ)
G=0.5 (3/6, Siberian)
T=0.5 (3/6, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
KRT39 : Missense Variant
LOC107985072 : 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 220720 G=0.983246 T=0.016754
European Sub 181374 G=0.989993 T=0.010007
African Sub 12688 G=0.93025 T=0.06975
African Others Sub 444 G=0.908 T=0.092
African American Sub 12244 G=0.93107 T=0.06893
Asian Sub 6294 G=0.9123 T=0.0877
East Asian Sub 4472 G=0.9195 T=0.0805
Other Asian Sub 1822 G=0.8946 T=0.1054
Latin American 1 Sub 812 G=0.979 T=0.021
Latin American 2 Sub 1008 G=0.9891 T=0.0109
South Asian Sub 292 G=0.973 T=0.027
Other Sub 18252 G=0.97754 T=0.02246


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=0.966327 T=0.033673
gnomAD - Exomes Global Study-wide 251314 G=0.979372 T=0.020628
gnomAD - Exomes European Sub 135256 G=0.990159 T=0.009841
gnomAD - Exomes Asian Sub 49006 G=0.95705 T=0.04295
gnomAD - Exomes American Sub 34586 G=0.98994 T=0.01006
gnomAD - Exomes African Sub 16256 G=0.92323 T=0.07677
gnomAD - Exomes Ashkenazi Jewish Sub 10080 G=0.99454 T=0.00546
gnomAD - Exomes Other Sub 6130 G=0.9842 T=0.0158
Allele Frequency Aggregator Total Global 204220 G=0.984203 T=0.015797
Allele Frequency Aggregator European Sub 171164 G=0.989951 T=0.010049
Allele Frequency Aggregator Other Sub 16800 G=0.97768 T=0.02232
Allele Frequency Aggregator African Sub 7850 G=0.9308 T=0.0692
Allele Frequency Aggregator Asian Sub 6294 G=0.9123 T=0.0877
Allele Frequency Aggregator Latin American 2 Sub 1008 G=0.9891 T=0.0109
Allele Frequency Aggregator Latin American 1 Sub 812 G=0.979 T=0.021
Allele Frequency Aggregator South Asian Sub 292 G=0.973 T=0.027
gnomAD - Genomes Global Study-wide 140206 G=0.969117 T=0.030883
gnomAD - Genomes European Sub 75940 G=0.99016 T=0.00984
gnomAD - Genomes African Sub 42008 G=0.93011 T=0.06989
gnomAD - Genomes American Sub 13658 G=0.98155 T=0.01845
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.9967 T=0.0033
gnomAD - Genomes East Asian Sub 3130 G=0.8949 T=0.1051
gnomAD - Genomes Other Sub 2150 G=0.9744 T=0.0256
ExAC Global Study-wide 121404 G=0.979383 T=0.020617
ExAC Europe Sub 73354 G=0.99134 T=0.00866
ExAC Asian Sub 25162 G=0.96193 T=0.03807
ExAC American Sub 11576 G=0.99076 T=0.00924
ExAC African Sub 10404 G=0.92474 T=0.07526
ExAC Other Sub 908 G=0.978 T=0.022
The PAGE Study Global Study-wide 78700 G=0.95177 T=0.04823
The PAGE Study AfricanAmerican Sub 32516 G=0.93090 T=0.06910
The PAGE Study Mexican Sub 10810 G=0.99019 T=0.00981
The PAGE Study Asian Sub 8318 G=0.9477 T=0.0523
The PAGE Study PuertoRican Sub 7918 G=0.9740 T=0.0260
The PAGE Study NativeHawaiian Sub 4534 G=0.9113 T=0.0887
The PAGE Study Cuban Sub 4230 G=0.9735 T=0.0265
The PAGE Study Dominican Sub 3828 G=0.9561 T=0.0439
The PAGE Study CentralAmerican Sub 2448 G=0.9775 T=0.0225
The PAGE Study SouthAmerican Sub 1982 G=0.9904 T=0.0096
The PAGE Study NativeAmerican Sub 1260 G=0.9738 T=0.0262
The PAGE Study SouthAsian Sub 856 G=0.985 T=0.015
14KJPN JAPANESE Study-wide 28258 G=0.95927 T=0.04073
8.3KJPN JAPANESE Study-wide 16760 G=0.95853 T=0.04147
GO Exome Sequencing Project Global Study-wide 12998 G=0.96984 T=0.03016
GO Exome Sequencing Project European American Sub 8592 G=0.9899 T=0.0101
GO Exome Sequencing Project African American Sub 4406 G=0.9308 T=0.0692
1000Genomes_30x Global Study-wide 6404 G=0.9517 T=0.0483
1000Genomes_30x African Sub 1786 G=0.9087 T=0.0913
1000Genomes_30x Europe Sub 1266 G=0.9874 T=0.0126
1000Genomes_30x South Asian Sub 1202 G=0.9892 T=0.0108
1000Genomes_30x East Asian Sub 1170 G=0.9094 T=0.0906
1000Genomes_30x American Sub 980 G=0.989 T=0.011
1000Genomes Global Study-wide 5008 G=0.9539 T=0.0461
1000Genomes African Sub 1322 G=0.9115 T=0.0885
1000Genomes East Asian Sub 1008 G=0.9157 T=0.0843
1000Genomes Europe Sub 1006 G=0.9881 T=0.0119
1000Genomes South Asian Sub 978 G=0.990 T=0.010
1000Genomes American Sub 694 G=0.990 T=0.010
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.9922 T=0.0078
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.9875 T=0.0125
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.9911 T=0.0089
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.9280 T=0.0720
HapMap Global Study-wide 1892 G=0.9424 T=0.0576
HapMap American Sub 770 G=0.952 T=0.048
HapMap African Sub 692 G=0.922 T=0.078
HapMap Asian Sub 254 G=0.937 T=0.063
HapMap Europe Sub 176 G=0.989 T=0.011
Genome-wide autozygosity in Daghestan Global Study-wide 1136 G=0.9903 T=0.0097
Genome-wide autozygosity in Daghestan Daghestan Sub 628 G=0.997 T=0.003
Genome-wide autozygosity in Daghestan Near_East Sub 144 G=0.986 T=0.014
Genome-wide autozygosity in Daghestan Central Asia Sub 122 G=0.967 T=0.033
Genome-wide autozygosity in Daghestan Europe Sub 108 G=0.972 T=0.028
Genome-wide autozygosity in Daghestan South Asian Sub 98 G=1.00 T=0.00
Genome-wide autozygosity in Daghestan Caucasus Sub 36 G=1.00 T=0.00
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.996 T=0.004
CNV burdens in cranial meningiomas Global Study-wide 792 G=0.913 T=0.087
CNV burdens in cranial meningiomas CRM Sub 792 G=0.913 T=0.087
Chileans Chilean Study-wide 626 G=0.994 T=0.006
A Vietnamese Genetic Variation Database Global Study-wide 612 G=0.908 T=0.092
Northern Sweden ACPOP Study-wide 600 G=0.998 T=0.002
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.987 T=0.013
FINRISK Finnish from FINRISK project Study-wide 304 G=0.993 T=0.007
Qatari Global Study-wide 216 G=0.991 T=0.009
SGDP_PRJ Global Study-wide 34 G=0.50 T=0.50
Siberian Global Study-wide 6 G=0.5 T=0.5
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 17 NC_000017.11:g.40960351G>T
GRCh37.p13 chr 17 NC_000017.10:g.39116603G>T
KRT39 RefSeqGene NG_012415.1:g.11542C>A
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4 NW_003871091.1:g.109746G>T
Gene: KRT39, keratin 39 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
KRT39 transcript NM_213656.4:c.1147C>A L [CTG] > M [ATG] Coding Sequence Variant
keratin, type I cytoskeletal 39 NP_998821.3:p.Leu383Met L (Leu) > M (Met) Missense Variant
Gene: LOC107985072, uncharacterized LOC107985072 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC107985072 transcript variant X2 XR_001752885.2:n. N/A Intron Variant
LOC107985072 transcript variant X1 XR_001752886.2:n. 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.

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= T
GRCh38.p14 chr 17 NC_000017.11:g.40960351= NC_000017.11:g.40960351G>T
GRCh37.p13 chr 17 NC_000017.10:g.39116603= NC_000017.10:g.39116603G>T
KRT39 RefSeqGene NG_012415.1:g.11542= NG_012415.1:g.11542C>A
KRT39 transcript NM_213656.4:c.1147= NM_213656.4:c.1147C>A
KRT39 transcript NM_213656.3:c.1147= NM_213656.3:c.1147C>A
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4 NW_003871091.1:g.109746= NW_003871091.1:g.109746G>T
keratin, type I cytoskeletal 39 NP_998821.3:p.Leu383= NP_998821.3:p.Leu383Met
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#.

94 SubSNP, 27 Frequency submissions
No Submitter Submission ID Date (Build)
1 PERLEGEN ss23626833 Sep 21, 2004 (123)
2 AFFY ss66264216 Dec 01, 2006 (127)
3 PERLEGEN ss69196201 May 17, 2007 (127)
4 AFFY ss76409223 Dec 07, 2007 (129)
5 KRIBB_YJKIM ss83289425 Dec 15, 2007 (131)
6 ILLUMINA ss161059125 Dec 01, 2009 (131)
7 COMPLETE_GENOMICS ss169597002 Jul 04, 2010 (132)
8 AFFY ss173498586 Jul 04, 2010 (132)
9 BUSHMAN ss202503580 Jul 04, 2010 (132)
10 1000GENOMES ss339688084 May 09, 2011 (134)
11 NHLBI-ESP ss342453107 May 09, 2011 (134)
12 ILLUMINA ss479432966 Sep 08, 2015 (146)
13 1000GENOMES ss491123069 May 04, 2012 (137)
14 EXOME_CHIP ss491521775 May 04, 2012 (137)
15 ILLUMINA ss536056907 Sep 08, 2015 (146)
16 TISHKOFF ss565266766 Apr 25, 2013 (138)
17 SSMP ss661069006 Apr 25, 2013 (138)
18 ILLUMINA ss780728213 Sep 08, 2015 (146)
19 ILLUMINA ss783404410 Sep 08, 2015 (146)
20 JMKIDD_LAB ss974498752 Aug 21, 2014 (142)
21 EVA-GONL ss993097946 Aug 21, 2014 (142)
22 JMKIDD_LAB ss1067571059 Aug 21, 2014 (142)
23 JMKIDD_LAB ss1081051758 Aug 21, 2014 (142)
24 1000GENOMES ss1358612091 Aug 21, 2014 (142)
25 HAMMER_LAB ss1397730314 Sep 08, 2015 (146)
26 EVA_FINRISK ss1584106037 Apr 01, 2015 (144)
27 EVA_UK10K_ALSPAC ss1635632142 Apr 01, 2015 (144)
28 EVA_UK10K_TWINSUK ss1678626175 Apr 01, 2015 (144)
29 EVA_EXAC ss1692763792 Apr 01, 2015 (144)
30 EVA_DECODE ss1697140377 Apr 01, 2015 (144)
31 EVA_MGP ss1711459808 Apr 01, 2015 (144)
32 EVA_SVP ss1713581874 Apr 01, 2015 (144)
33 ILLUMINA ss1752224851 Sep 08, 2015 (146)
34 ILLUMINA ss1917918106 Feb 12, 2016 (147)
35 WEILL_CORNELL_DGM ss1936557046 Feb 12, 2016 (147)
36 ILLUMINA ss1946446150 Feb 12, 2016 (147)
37 ILLUMINA ss1959745442 Feb 12, 2016 (147)
38 JJLAB ss2029056428 Sep 14, 2016 (149)
39 USC_VALOUEV ss2157525266 Dec 20, 2016 (150)
40 HUMAN_LONGEVITY ss2216762559 Dec 20, 2016 (150)
41 GRF ss2702086661 Nov 08, 2017 (151)
42 GNOMAD ss2742695049 Nov 08, 2017 (151)
43 GNOMAD ss2749767490 Nov 08, 2017 (151)
44 GNOMAD ss2949746119 Nov 08, 2017 (151)
45 AFFY ss2985094837 Nov 08, 2017 (151)
46 SWEGEN ss3015516197 Nov 08, 2017 (151)
47 ILLUMINA ss3021778364 Nov 08, 2017 (151)
48 CSHL ss3351741915 Nov 08, 2017 (151)
49 ILLUMINA ss3625709189 Oct 12, 2018 (152)
50 ILLUMINA ss3627666900 Oct 12, 2018 (152)
51 ILLUMINA ss3627666901 Oct 12, 2018 (152)
52 ILLUMINA ss3634674453 Oct 12, 2018 (152)
53 ILLUMINA ss3636364509 Oct 12, 2018 (152)
54 ILLUMINA ss3640381766 Oct 12, 2018 (152)
55 ILLUMINA ss3644687660 Oct 12, 2018 (152)
56 ILLUMINA ss3652194422 Oct 12, 2018 (152)
57 ILLUMINA ss3653866622 Oct 12, 2018 (152)
58 EGCUT_WGS ss3682407392 Jul 13, 2019 (153)
59 EVA_DECODE ss3700444937 Jul 13, 2019 (153)
60 ILLUMINA ss3725620126 Jul 13, 2019 (153)
61 ACPOP ss3742017549 Jul 13, 2019 (153)
62 ILLUMINA ss3744443395 Jul 13, 2019 (153)
63 ILLUMINA ss3744974751 Jul 13, 2019 (153)
64 EVA ss3754654527 Jul 13, 2019 (153)
65 PAGE_CC ss3771926736 Jul 13, 2019 (153)
66 ILLUMINA ss3772472647 Jul 13, 2019 (153)
67 KHV_HUMAN_GENOMES ss3819925311 Jul 13, 2019 (153)
68 EVA ss3825110993 Apr 27, 2020 (154)
69 EVA ss3825898859 Apr 27, 2020 (154)
70 SGDP_PRJ ss3885727820 Apr 27, 2020 (154)
71 KRGDB ss3935407400 Apr 27, 2020 (154)
72 EVA ss3984722994 Apr 26, 2021 (155)
73 EVA ss3986725984 Apr 26, 2021 (155)
74 TOPMED ss5035618695 Apr 26, 2021 (155)
75 TOMMO_GENOMICS ss5222363444 Apr 26, 2021 (155)
76 EVA ss5236942623 Apr 26, 2021 (155)
77 EVA ss5237575387 Apr 26, 2021 (155)
78 1000G_HIGH_COVERAGE ss5303095070 Oct 16, 2022 (156)
79 EVA ss5315886119 Oct 16, 2022 (156)
80 EVA ss5427528856 Oct 16, 2022 (156)
81 HUGCELL_USP ss5496156814 Oct 16, 2022 (156)
82 EVA ss5511763219 Oct 16, 2022 (156)
83 1000G_HIGH_COVERAGE ss5606797530 Oct 16, 2022 (156)
84 SANFORD_IMAGENETICS ss5624397014 Oct 16, 2022 (156)
85 SANFORD_IMAGENETICS ss5660082525 Oct 16, 2022 (156)
86 TOMMO_GENOMICS ss5778554216 Oct 16, 2022 (156)
87 YY_MCH ss5816533795 Oct 16, 2022 (156)
88 EVA ss5833968850 Oct 16, 2022 (156)
89 EVA ss5847796823 Oct 16, 2022 (156)
90 EVA ss5848448745 Oct 16, 2022 (156)
91 EVA ss5851804466 Oct 16, 2022 (156)
92 EVA ss5913917086 Oct 16, 2022 (156)
93 EVA ss5951476501 Oct 16, 2022 (156)
94 EVA ss5979506666 Oct 16, 2022 (156)
95 1000Genomes NC_000017.10 - 39116603 Oct 12, 2018 (152)
96 1000Genomes_30x NC_000017.11 - 40960351 Oct 16, 2022 (156)
97 The Avon Longitudinal Study of Parents and Children NC_000017.10 - 39116603 Oct 12, 2018 (152)
98 Chileans NC_000017.10 - 39116603 Apr 27, 2020 (154)
99 Genome-wide autozygosity in Daghestan NC_000017.9 - 36370129 Apr 27, 2020 (154)
100 Genetic variation in the Estonian population NC_000017.10 - 39116603 Oct 12, 2018 (152)
101 ExAC NC_000017.10 - 39116603 Oct 12, 2018 (152)
102 FINRISK NC_000017.10 - 39116603 Apr 27, 2020 (154)
103 gnomAD - Genomes NC_000017.11 - 40960351 Apr 26, 2021 (155)
104 gnomAD - Exomes NC_000017.10 - 39116603 Jul 13, 2019 (153)
105 GO Exome Sequencing Project NC_000017.10 - 39116603 Oct 12, 2018 (152)
106 Genome of the Netherlands Release 5 NC_000017.10 - 39116603 Apr 27, 2020 (154)
107 HapMap NC_000017.11 - 40960351 Apr 27, 2020 (154)
108 KOREAN population from KRGDB NC_000017.10 - 39116603 Apr 27, 2020 (154)
109 Medical Genome Project healthy controls from Spanish population NC_000017.10 - 39116603 Apr 27, 2020 (154)
110 Northern Sweden NC_000017.10 - 39116603 Jul 13, 2019 (153)
111 The PAGE Study NC_000017.11 - 40960351 Jul 13, 2019 (153)
112 CNV burdens in cranial meningiomas NC_000017.10 - 39116603 Apr 26, 2021 (155)
113 Qatari NC_000017.10 - 39116603 Apr 27, 2020 (154)
114 SGDP_PRJ NC_000017.10 - 39116603 Apr 27, 2020 (154)
115 Siberian NC_000017.10 - 39116603 Apr 27, 2020 (154)
116 8.3KJPN NC_000017.10 - 39116603 Apr 26, 2021 (155)
117 14KJPN NC_000017.11 - 40960351 Oct 16, 2022 (156)
118 TopMed NC_000017.11 - 40960351 Apr 26, 2021 (155)
119 UK 10K study - Twins NC_000017.10 - 39116603 Oct 12, 2018 (152)
120 A Vietnamese Genetic Variation Database NC_000017.10 - 39116603 Jul 13, 2019 (153)
121 ALFA NC_000017.11 - 40960351 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)
rs59369178 Dec 02, 2009 (131)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
200196, ss66264216, ss76409223, ss169597002, ss173498586, ss202503580, ss1397730314, ss1697140377, ss1713581874 NC_000017.9:36370128:G:T NC_000017.11:40960350:G:T (self)
71852274, 39825502, 181215, 28145640, 3205993, 102498, 11997744, 1568101, 17750652, 42584794, 575568, 15302414, 272540, 18598968, 37744800, 10041620, 80332751, 39825502, 8813637, ss339688084, ss342453107, ss479432966, ss491123069, ss491521775, ss536056907, ss565266766, ss661069006, ss780728213, ss783404410, ss974498752, ss993097946, ss1067571059, ss1081051758, ss1358612091, ss1584106037, ss1635632142, ss1678626175, ss1692763792, ss1711459808, ss1752224851, ss1917918106, ss1936557046, ss1946446150, ss1959745442, ss2029056428, ss2157525266, ss2702086661, ss2742695049, ss2749767490, ss2949746119, ss2985094837, ss3015516197, ss3021778364, ss3351741915, ss3625709189, ss3627666900, ss3627666901, ss3634674453, ss3636364509, ss3640381766, ss3644687660, ss3652194422, ss3653866622, ss3682407392, ss3742017549, ss3744443395, ss3744974751, ss3754654527, ss3772472647, ss3825110993, ss3825898859, ss3885727820, ss3935407400, ss3984722994, ss3986725984, ss5222363444, ss5237575387, ss5315886119, ss5427528856, ss5511763219, ss5624397014, ss5660082525, ss5833968850, ss5847796823, ss5848448745, ss5951476501, ss5979506666 NC_000017.10:39116602:G:T NC_000017.11:40960350:G:T (self)
94323465, 506928595, 1486733, 1148205, 112391320, 251164357, 8276006261, ss2216762559, ss3700444937, ss3725620126, ss3771926736, ss3819925311, ss5035618695, ss5236942623, ss5303095070, ss5496156814, ss5606797530, ss5778554216, ss5816533795, ss5851804466, ss5913917086 NC_000017.11:40960350:G:T NC_000017.11:40960350:G:T (self)
ss23626833, ss69196201, ss83289425, ss161059125 NT_010783.15:4390754:G:T NC_000017.11:40960350:G: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 rs17843023

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