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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.

rs9383932

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:151598585 (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
A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.153935 (40745/264690, TOPMED)
G=0.149345 (30627/205076, GENOGRAPHIC)
G=0.133313 (19087/143174, ALFA) (+ 21 more)
G=0.150089 (21025/140084, GnomAD)
G=0.33927 (9587/28258, 14KJPN)
G=0.34159 (5725/16760, 8.3KJPN)
G=0.1821 (1166/6404, 1000G_30x)
G=0.1883 (943/5008, 1000G)
G=0.1132 (507/4480, Estonian)
G=0.1445 (557/3854, ALSPAC)
G=0.1570 (582/3708, TWINSUK)
G=0.3621 (1061/2930, KOREAN)
G=0.2049 (427/2084, HGDP_Stanford)
G=0.1792 (339/1892, HapMap)
G=0.3614 (662/1832, Korea1K)
G=0.1226 (139/1134, Daghestan)
G=0.154 (154/998, GoNL)
G=0.075 (47/626, Chileans)
G=0.095 (57/600, NorthernSweden)
G=0.185 (40/216, Qatari)
A=0.409 (85/208, SGDP_PRJ)
G=0.08 (4/50, Ancient Sardinia)
G=0.12 (5/40, GENOME_DK)
A=0.4 (3/8, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CCDC170 : Intron Variant
Publications
1 citation
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 143174 A=0.866687 G=0.133313, T=0.000000
European Sub 115198 A=0.864451 G=0.135549, T=0.000000
African Sub 6742 A=0.8846 G=0.1154, T=0.0000
African Others Sub 236 A=0.869 G=0.131, T=0.000
African American Sub 6506 A=0.8852 G=0.1148, T=0.0000
Asian Sub 642 A=0.656 G=0.344, T=0.000
East Asian Sub 500 A=0.664 G=0.336, T=0.000
Other Asian Sub 142 A=0.627 G=0.373, T=0.000
Latin American 1 Sub 876 A=0.862 G=0.138, T=0.000
Latin American 2 Sub 8434 A=0.9227 G=0.0773, T=0.0000
South Asian Sub 5022 A=0.8401 G=0.1599, T=0.0000
Other Sub 6260 A=0.8567 G=0.1433, T=0.0000


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 A=0.846065 G=0.153935
Genographic Project Global Study-wide 205076 A=0.850655 G=0.149345, T=0.000000
Allele Frequency Aggregator Total Global 143174 A=0.866687 G=0.133313, T=0.000000
Allele Frequency Aggregator European Sub 115198 A=0.864451 G=0.135549, T=0.000000
Allele Frequency Aggregator Latin American 2 Sub 8434 A=0.9227 G=0.0773, T=0.0000
Allele Frequency Aggregator African Sub 6742 A=0.8846 G=0.1154, T=0.0000
Allele Frequency Aggregator Other Sub 6260 A=0.8567 G=0.1433, T=0.0000
Allele Frequency Aggregator South Asian Sub 5022 A=0.8401 G=0.1599, T=0.0000
Allele Frequency Aggregator Latin American 1 Sub 876 A=0.862 G=0.138, T=0.000
Allele Frequency Aggregator Asian Sub 642 A=0.656 G=0.344, T=0.000
gnomAD - Genomes Global Study-wide 140084 A=0.849911 G=0.150089
gnomAD - Genomes European Sub 75890 A=0.86126 G=0.13874
gnomAD - Genomes African Sub 41960 A=0.84123 G=0.15877
gnomAD - Genomes American Sub 13638 A=0.88026 G=0.11974
gnomAD - Genomes Ashkenazi Jewish Sub 3320 A=0.8172 G=0.1828
gnomAD - Genomes East Asian Sub 3124 A=0.6069 G=0.3931
gnomAD - Genomes Other Sub 2152 A=0.8299 G=0.1701
14KJPN JAPANESE Study-wide 28258 A=0.66073 G=0.33927
8.3KJPN JAPANESE Study-wide 16760 A=0.65841 G=0.34159
1000Genomes_30x Global Study-wide 6404 A=0.8179 G=0.1821
1000Genomes_30x African Sub 1786 A=0.8466 G=0.1534
1000Genomes_30x Europe Sub 1266 A=0.8665 G=0.1335
1000Genomes_30x South Asian Sub 1202 A=0.8444 G=0.1556
1000Genomes_30x East Asian Sub 1170 A=0.6197 G=0.3803
1000Genomes_30x American Sub 980 A=0.907 G=0.093
1000Genomes Global Study-wide 5008 A=0.8117 G=0.1883
1000Genomes African Sub 1322 A=0.8502 G=0.1498
1000Genomes East Asian Sub 1008 A=0.6141 G=0.3859
1000Genomes Europe Sub 1006 A=0.8688 G=0.1312
1000Genomes South Asian Sub 978 A=0.840 G=0.160
1000Genomes American Sub 694 A=0.902 G=0.098
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.8868 G=0.1132
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.8555 G=0.1445
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.8430 G=0.1570
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.6379 G=0.3621
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.7951 G=0.2049
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.681 G=0.319
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.819 G=0.181
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.831 G=0.169
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.856 G=0.144
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.756 G=0.244
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.981 G=0.019
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.53 G=0.47
HapMap Global Study-wide 1892 A=0.8208 G=0.1792
HapMap American Sub 770 A=0.808 G=0.192
HapMap African Sub 692 A=0.880 G=0.120
HapMap Asian Sub 254 A=0.677 G=0.323
HapMap Europe Sub 176 A=0.852 G=0.148
Korean Genome Project KOREAN Study-wide 1832 A=0.6386 G=0.3614
Genome-wide autozygosity in Daghestan Global Study-wide 1134 A=0.8774 G=0.1226
Genome-wide autozygosity in Daghestan Daghestan Sub 628 A=0.887 G=0.113
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.889 G=0.111
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.820 G=0.180
Genome-wide autozygosity in Daghestan Europe Sub 108 A=0.861 G=0.139
Genome-wide autozygosity in Daghestan South Asian Sub 96 A=0.86 G=0.14
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.94 G=0.06
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.846 G=0.154
Chileans Chilean Study-wide 626 A=0.925 G=0.075
Northern Sweden ACPOP Study-wide 600 A=0.905 G=0.095
Qatari Global Study-wide 216 A=0.815 G=0.185
SGDP_PRJ Global Study-wide 208 A=0.409 G=0.591
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 50 A=0.92 G=0.08
The Danish reference pan genome Danish Study-wide 40 A=0.88 G=0.12
Siberian Global Study-wide 8 A=0.4 G=0.6
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 6 NC_000006.12:g.151598585A>G
GRCh38.p14 chr 6 NC_000006.12:g.151598585A>T
GRCh37.p13 chr 6 NC_000006.11:g.151919720A>G
GRCh37.p13 chr 6 NC_000006.11:g.151919720A>T
CCDC170 RefSeqGene NG_021198.1:g.109546A>G
CCDC170 RefSeqGene NG_021198.1:g.109546A>T
Gene: CCDC170, coiled-coil domain containing 170 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
CCDC170 transcript NM_025059.4:c.1710+2008A>G N/A Intron Variant
CCDC170 transcript variant X1 XM_011536147.3:c.1728+200…

XM_011536147.3:c.1728+2008A>G

N/A Intron Variant
CCDC170 transcript variant X2 XM_011536148.3:c.1527+200…

XM_011536148.3:c.1527+2008A>G

N/A Intron Variant
CCDC170 transcript variant X3 XM_047419372.1:c.1509+200…

XM_047419372.1:c.1509+2008A>G

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 A= G T
GRCh38.p14 chr 6 NC_000006.12:g.151598585= NC_000006.12:g.151598585A>G NC_000006.12:g.151598585A>T
GRCh37.p13 chr 6 NC_000006.11:g.151919720= NC_000006.11:g.151919720A>G NC_000006.11:g.151919720A>T
CCDC170 RefSeqGene NG_021198.1:g.109546= NG_021198.1:g.109546A>G NG_021198.1:g.109546A>T
CCDC170 transcript NM_025059.3:c.1710+2008= NM_025059.3:c.1710+2008A>G NM_025059.3:c.1710+2008A>T
CCDC170 transcript NM_025059.4:c.1710+2008= NM_025059.4:c.1710+2008A>G NM_025059.4:c.1710+2008A>T
CCDC170 transcript variant X1 XM_011536147.3:c.1728+2008= XM_011536147.3:c.1728+2008A>G XM_011536147.3:c.1728+2008A>T
CCDC170 transcript variant X2 XM_011536148.3:c.1527+2008= XM_011536148.3:c.1527+2008A>G XM_011536148.3:c.1527+2008A>T
CCDC170 transcript variant X3 XM_047419372.1:c.1509+2008= XM_047419372.1:c.1509+2008A>G XM_047419372.1:c.1509+2008A>T
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#.

104 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_SNP ss12873200 Dec 05, 2003 (119)
2 SC_SNP ss15726242 Feb 27, 2004 (120)
3 AFFY ss66262950 Nov 29, 2006 (127)
4 ILLUMINA ss67912735 Nov 29, 2006 (127)
5 ILLUMINA ss68039919 Nov 29, 2006 (127)
6 ILLUMINA ss68302459 Dec 12, 2006 (127)
7 PERLEGEN ss68996156 May 17, 2007 (127)
8 ILLUMINA ss71604584 May 17, 2007 (127)
9 ILLUMINA ss75549080 Dec 07, 2007 (129)
10 AFFY ss76408095 Dec 07, 2007 (129)
11 HGSV ss82417408 Dec 14, 2007 (130)
12 KRIBB_YJKIM ss84813647 Dec 14, 2007 (130)
13 ILLUMINA ss98254256 May 24, 2008 (130)
14 BGI ss104374223 Dec 01, 2009 (131)
15 ILLUMINA-UK ss116771963 Feb 14, 2009 (130)
16 ILLUMINA ss154491275 Dec 01, 2009 (131)
17 GMI ss157746854 Dec 01, 2009 (131)
18 ILLUMINA ss159665299 Dec 01, 2009 (131)
19 ILLUMINA ss160983113 Dec 01, 2009 (131)
20 AFFY ss173495773 Jul 04, 2010 (132)
21 ILLUMINA ss174831324 Jul 04, 2010 (132)
22 BUSHMAN ss202593026 Jul 04, 2010 (132)
23 BCM-HGSC-SUB ss207721770 Jul 04, 2010 (132)
24 1000GENOMES ss222759289 Jul 14, 2010 (132)
25 1000GENOMES ss233741600 Jul 15, 2010 (132)
26 1000GENOMES ss240745187 Jul 15, 2010 (132)
27 GMI ss279079483 May 04, 2012 (137)
28 PJP ss293761390 May 09, 2011 (134)
29 ILLUMINA ss481886562 May 04, 2012 (137)
30 ILLUMINA ss481919580 May 04, 2012 (137)
31 ILLUMINA ss482877867 Sep 08, 2015 (146)
32 ILLUMINA ss485737476 May 04, 2012 (137)
33 ILLUMINA ss537593718 Sep 08, 2015 (146)
34 TISHKOFF ss559624836 Apr 25, 2013 (138)
35 SSMP ss653967040 Apr 25, 2013 (138)
36 ILLUMINA ss779008793 Sep 08, 2015 (146)
37 ILLUMINA ss783314460 Sep 08, 2015 (146)
38 ILLUMINA ss784266512 Sep 08, 2015 (146)
39 ILLUMINA ss832575955 Sep 08, 2015 (146)
40 ILLUMINA ss833176054 Jul 13, 2019 (153)
41 ILLUMINA ss834471245 Sep 08, 2015 (146)
42 EVA-GONL ss983661064 Aug 21, 2014 (142)
43 JMKIDD_LAB ss1074155964 Aug 21, 2014 (142)
44 1000GENOMES ss1322891875 Aug 21, 2014 (142)
45 HAMMER_LAB ss1397475873 Sep 08, 2015 (146)
46 DDI ss1430938984 Apr 01, 2015 (144)
47 EVA_GENOME_DK ss1581956385 Apr 01, 2015 (144)
48 EVA_DECODE ss1593237029 Apr 01, 2015 (144)
49 EVA_UK10K_ALSPAC ss1617030458 Apr 01, 2015 (144)
50 EVA_UK10K_TWINSUK ss1660024491 Apr 01, 2015 (144)
51 EVA_SVP ss1712911566 Apr 01, 2015 (144)
52 HAMMER_LAB ss1804740326 Sep 08, 2015 (146)
53 WEILL_CORNELL_DGM ss1926904754 Feb 12, 2016 (147)
54 JJLAB ss2024115585 Sep 14, 2016 (149)
55 USC_VALOUEV ss2152306546 Dec 20, 2016 (150)
56 HUMAN_LONGEVITY ss2289682660 Dec 20, 2016 (150)
57 SYSTEMSBIOZJU ss2626548093 Nov 08, 2017 (151)
58 ILLUMINA ss2635163852 Nov 08, 2017 (151)
59 GRF ss2707943769 Nov 08, 2017 (151)
60 GNOMAD ss2846874005 Nov 08, 2017 (151)
61 SWEGEN ss3000193698 Nov 08, 2017 (151)
62 BIOINF_KMB_FNS_UNIBA ss3025847446 Nov 08, 2017 (151)
63 CSHL ss3347296614 Nov 08, 2017 (151)
64 ILLUMINA ss3629690515 Oct 12, 2018 (152)
65 ILLUMINA ss3632442815 Oct 12, 2018 (152)
66 ILLUMINA ss3633442831 Oct 12, 2018 (152)
67 ILLUMINA ss3634166645 Oct 12, 2018 (152)
68 ILLUMINA ss3636823937 Oct 12, 2018 (152)
69 ILLUMINA ss3638665688 Oct 12, 2018 (152)
70 ILLUMINA ss3639334304 Oct 12, 2018 (152)
71 ILLUMINA ss3639962140 Oct 12, 2018 (152)
72 ILLUMINA ss3641204253 Oct 12, 2018 (152)
73 ILLUMINA ss3641501569 Oct 12, 2018 (152)
74 ILLUMINA ss3643604150 Oct 12, 2018 (152)
75 ILLUMINA ss3644006681 Oct 12, 2018 (152)
76 EGCUT_WGS ss3668130259 Jul 13, 2019 (153)
77 EVA_DECODE ss3718580040 Jul 13, 2019 (153)
78 ACPOP ss3734116519 Jul 13, 2019 (153)
79 EVA ss3765859476 Jul 13, 2019 (153)
80 KHV_HUMAN_GENOMES ss3809020498 Jul 13, 2019 (153)
81 EVA ss3830268737 Apr 26, 2020 (154)
82 EVA ss3838619355 Apr 26, 2020 (154)
83 EVA ss3844069117 Apr 26, 2020 (154)
84 HGDP ss3847856522 Apr 26, 2020 (154)
85 SGDP_PRJ ss3866033949 Apr 26, 2020 (154)
86 KRGDB ss3913013129 Apr 26, 2020 (154)
87 KOGIC ss3960366026 Apr 26, 2020 (154)
88 EVA ss3985261926 Apr 26, 2021 (155)
89 TOPMED ss4727183683 Apr 26, 2021 (155)
90 TOMMO_GENOMICS ss5180619023 Apr 26, 2021 (155)
91 1000G_HIGH_COVERAGE ss5270892989 Oct 13, 2022 (156)
92 GENOGRAPHIC ss5314517463 Oct 13, 2022 (156)
93 EVA ss5370000796 Oct 13, 2022 (156)
94 HUGCELL_USP ss5468287605 Oct 13, 2022 (156)
95 1000G_HIGH_COVERAGE ss5558109292 Oct 13, 2022 (156)
96 SANFORD_IMAGENETICS ss5641803465 Oct 13, 2022 (156)
97 TOMMO_GENOMICS ss5719697849 Oct 13, 2022 (156)
98 EVA ss5799706983 Oct 13, 2022 (156)
99 YY_MCH ss5808091766 Oct 13, 2022 (156)
100 EVA ss5843200564 Oct 13, 2022 (156)
101 EVA ss5855647266 Oct 13, 2022 (156)
102 EVA ss5886581389 Oct 13, 2022 (156)
103 EVA ss5970750736 Oct 13, 2022 (156)
104 EVA ss5970750737 Oct 13, 2022 (156)
105 1000Genomes NC_000006.11 - 151919720 Oct 12, 2018 (152)
106 1000Genomes_30x NC_000006.12 - 151598585 Oct 13, 2022 (156)
107 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 151919720 Oct 12, 2018 (152)
108 Chileans NC_000006.11 - 151919720 Apr 26, 2020 (154)
109 Genome-wide autozygosity in Daghestan NC_000006.10 - 151961413 Apr 26, 2020 (154)
110 Genetic variation in the Estonian population NC_000006.11 - 151919720 Oct 12, 2018 (152)
111 Genographic Project NC_000006.12 - 151598585 Oct 13, 2022 (156)
112 The Danish reference pan genome NC_000006.11 - 151919720 Apr 26, 2020 (154)
113 gnomAD - Genomes NC_000006.12 - 151598585 Apr 26, 2021 (155)
114 Genome of the Netherlands Release 5 NC_000006.11 - 151919720 Apr 26, 2020 (154)
115 HGDP-CEPH-db Supplement 1 NC_000006.10 - 151961413 Apr 26, 2020 (154)
116 HapMap NC_000006.12 - 151598585 Apr 26, 2020 (154)
117 KOREAN population from KRGDB NC_000006.11 - 151919720 Apr 26, 2020 (154)
118 Korean Genome Project NC_000006.12 - 151598585 Apr 26, 2020 (154)
119 Northern Sweden NC_000006.11 - 151919720 Jul 13, 2019 (153)
120 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000006.11 - 151919720 Apr 26, 2021 (155)
121 Qatari NC_000006.11 - 151919720 Apr 26, 2020 (154)
122 SGDP_PRJ NC_000006.11 - 151919720 Apr 26, 2020 (154)
123 Siberian NC_000006.11 - 151919720 Apr 26, 2020 (154)
124 8.3KJPN NC_000006.11 - 151919720 Apr 26, 2021 (155)
125 14KJPN NC_000006.12 - 151598585 Oct 13, 2022 (156)
126 TopMed NC_000006.12 - 151598585 Apr 26, 2021 (155)
127 UK 10K study - Twins NC_000006.11 - 151919720 Oct 12, 2018 (152)
128 ALFA NC_000006.12 - 151598585 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)
rs58092979 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss82417408, ss3639334304, ss3639962140, ss3644006681 NC_000006.9:152011833:A:G NC_000006.12:151598584:A:G (self)
450241, 534414, ss66262950, ss76408095, ss116771963, ss173495773, ss202593026, ss207721770, ss279079483, ss293761390, ss481886562, ss1397475873, ss1593237029, ss1712911566, ss2635163852, ss3643604150, ss3847856522 NC_000006.10:151961412:A:G NC_000006.12:151598584:A:G (self)
34784115, 19394357, 394717, 13868507, 8121324, 8632195, 20190523, 7401384, 487853, 8946684, 18050929, 4822900, 38588330, 19394357, ss222759289, ss233741600, ss240745187, ss481919580, ss482877867, ss485737476, ss537593718, ss559624836, ss653967040, ss779008793, ss783314460, ss784266512, ss832575955, ss833176054, ss834471245, ss983661064, ss1074155964, ss1322891875, ss1430938984, ss1581956385, ss1617030458, ss1660024491, ss1804740326, ss1926904754, ss2024115585, ss2152306546, ss2626548093, ss2707943769, ss2846874005, ss3000193698, ss3347296614, ss3629690515, ss3632442815, ss3633442831, ss3634166645, ss3636823937, ss3638665688, ss3641204253, ss3641501569, ss3668130259, ss3734116519, ss3765859476, ss3830268737, ss3838619355, ss3866033949, ss3913013129, ss3985261926, ss5180619023, ss5370000796, ss5641803465, ss5799706983, ss5843200564, ss5970750736, ss5970750737 NC_000006.11:151919719:A:G NC_000006.12:151598584:A:G (self)
45635227, 122006, 245593561, 3283262, 16744027, 53534953, 564561241, 10837597048, ss2289682660, ss3025847446, ss3718580040, ss3809020498, ss3844069117, ss3960366026, ss4727183683, ss5270892989, ss5314517463, ss5468287605, ss5558109292, ss5719697849, ss5808091766, ss5855647266, ss5886581389 NC_000006.12:151598584:A:G NC_000006.12:151598584:A:G (self)
ss12873200 NT_023451.12:1893176:A:G NC_000006.12:151598584:A:G (self)
ss15726242 NT_025741.13:56074569:A:G NC_000006.12:151598584:A:G (self)
ss67912735, ss68039919, ss68302459, ss68996156, ss71604584, ss75549080, ss84813647, ss98254256, ss104374223, ss154491275, ss157746854, ss159665299, ss160983113, ss174831324 NT_025741.15:56089176:A:G NC_000006.12:151598584:A:G (self)
122006, 10837597048, ss5314517463 NC_000006.12:151598584:A:T NC_000006.12:151598584:A:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs9383932
PMID Title Author Year Journal
20661439 Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus. Stacey SN et al. 2010 PLoS genetics
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