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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.

rs10956365

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr8:127391642 (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>A / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.150405 (21075/140122, GnomAD)
A=0.169233 (21560/127398, ALFA)
A=0.09392 (7391/78698, PAGE_STUDY) (+ 19 more)
A=0.06126 (1731/28258, 14KJPN)
A=0.06002 (1006/16760, 8.3KJPN)
A=0.1168 (748/6404, 1000G_30x)
A=0.1192 (597/5008, 1000G)
A=0.2116 (948/4480, Estonian)
A=0.1943 (749/3854, ALSPAC)
A=0.1915 (710/3708, TWINSUK)
A=0.0791 (231/2922, KOREAN)
A=0.1427 (297/2082, HGDP_Stanford)
A=0.1115 (211/1892, HapMap)
A=0.2257 (256/1134, Daghestan)
A=0.205 (205/998, GoNL)
A=0.227 (136/600, NorthernSweden)
A=0.116 (25/216, Qatari)
A=0.189 (40/212, Vietnamese)
G=0.452 (75/166, SGDP_PRJ)
A=0.06 (4/70, Ancient Sardinia)
A=0.17 (7/40, GENOME_DK)
G=0.41 (9/22, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CASC8 : Intron Variant
CASC21 : Intron Variant
Publications
2 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 127398 G=0.830767 A=0.169233, T=0.000000
European Sub 105012 G=0.817078 A=0.182922, T=0.000000
African Sub 9508 G=0.9531 A=0.0469, T=0.0000
African Others Sub 324 G=0.978 A=0.022, T=0.000
African American Sub 9184 G=0.9522 A=0.0478, T=0.0000
Asian Sub 576 G=0.908 A=0.092, T=0.000
East Asian Sub 500 G=0.914 A=0.086, T=0.000
Other Asian Sub 76 G=0.87 A=0.13, T=0.00
Latin American 1 Sub 602 G=0.877 A=0.123, T=0.000
Latin American 2 Sub 1468 G=0.9332 A=0.0668, T=0.0000
South Asian Sub 5020 G=0.8430 A=0.1570, T=0.0000
Other Sub 5212 G=0.8289 A=0.1711, 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
gnomAD - Genomes Global Study-wide 140122 G=0.849595 A=0.150405
gnomAD - Genomes European Sub 75878 G=0.79563 A=0.20437
gnomAD - Genomes African Sub 41992 G=0.93966 A=0.06034
gnomAD - Genomes American Sub 13648 G=0.88965 A=0.11035
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.7899 A=0.2101
gnomAD - Genomes East Asian Sub 3134 G=0.8417 A=0.1583
gnomAD - Genomes Other Sub 2148 G=0.8445 A=0.1555
Allele Frequency Aggregator Total Global 127398 G=0.830767 A=0.169233, T=0.000000
Allele Frequency Aggregator European Sub 105012 G=0.817078 A=0.182922, T=0.000000
Allele Frequency Aggregator African Sub 9508 G=0.9531 A=0.0469, T=0.0000
Allele Frequency Aggregator Other Sub 5212 G=0.8289 A=0.1711, T=0.0000
Allele Frequency Aggregator South Asian Sub 5020 G=0.8430 A=0.1570, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 1468 G=0.9332 A=0.0668, T=0.0000
Allele Frequency Aggregator Latin American 1 Sub 602 G=0.877 A=0.123, T=0.000
Allele Frequency Aggregator Asian Sub 576 G=0.908 A=0.092, T=0.000
The PAGE Study Global Study-wide 78698 G=0.90608 A=0.09392
The PAGE Study AfricanAmerican Sub 32512 G=0.93664 A=0.06336
The PAGE Study Mexican Sub 10810 G=0.91563 A=0.08437
The PAGE Study Asian Sub 8318 G=0.9193 A=0.0807
The PAGE Study PuertoRican Sub 7918 G=0.8680 A=0.1320
The PAGE Study NativeHawaiian Sub 4534 G=0.7788 A=0.2212
The PAGE Study Cuban Sub 4230 G=0.8409 A=0.1591
The PAGE Study Dominican Sub 3828 G=0.9080 A=0.0920
The PAGE Study CentralAmerican Sub 2450 G=0.9212 A=0.0788
The PAGE Study SouthAmerican Sub 1982 G=0.9152 A=0.0848
The PAGE Study NativeAmerican Sub 1260 G=0.8437 A=0.1563
The PAGE Study SouthAsian Sub 856 G=0.863 A=0.137
14KJPN JAPANESE Study-wide 28258 G=0.93874 A=0.06126
8.3KJPN JAPANESE Study-wide 16760 G=0.93998 A=0.06002
1000Genomes_30x Global Study-wide 6404 G=0.8832 A=0.1168
1000Genomes_30x African Sub 1786 G=0.9681 A=0.0319
1000Genomes_30x Europe Sub 1266 G=0.7970 A=0.2030
1000Genomes_30x South Asian Sub 1202 G=0.8710 A=0.1290
1000Genomes_30x East Asian Sub 1170 G=0.8368 A=0.1632
1000Genomes_30x American Sub 980 G=0.910 A=0.090
1000Genomes Global Study-wide 5008 G=0.8808 A=0.1192
1000Genomes African Sub 1322 G=0.9682 A=0.0318
1000Genomes East Asian Sub 1008 G=0.8373 A=0.1627
1000Genomes Europe Sub 1006 G=0.7982 A=0.2018
1000Genomes South Asian Sub 978 G=0.872 A=0.128
1000Genomes American Sub 694 G=0.909 A=0.091
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7884 A=0.2116
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.8057 A=0.1943
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.8085 A=0.1915
KOREAN population from KRGDB KOREAN Study-wide 2922 G=0.9209 A=0.0791
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 G=0.8573 A=0.1427
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.853 A=0.147
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.848 A=0.152
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.831 A=0.169
HGDP-CEPH-db Supplement 1 Europe Sub 318 G=0.827 A=0.173
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.959 A=0.041
HGDP-CEPH-db Supplement 1 America Sub 216 G=1.000 A=0.000
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.43 A=0.57
HapMap Global Study-wide 1892 G=0.8885 A=0.1115
HapMap American Sub 770 G=0.860 A=0.140
HapMap African Sub 692 G=0.938 A=0.062
HapMap Asian Sub 254 G=0.890 A=0.110
HapMap Europe Sub 176 G=0.818 A=0.182
Genome-wide autozygosity in Daghestan Global Study-wide 1134 G=0.7743 A=0.2257
Genome-wide autozygosity in Daghestan Daghestan Sub 628 G=0.732 A=0.268
Genome-wide autozygosity in Daghestan Near_East Sub 144 G=0.764 A=0.236
Genome-wide autozygosity in Daghestan Central Asia Sub 120 G=0.850 A=0.150
Genome-wide autozygosity in Daghestan Europe Sub 108 G=0.843 A=0.157
Genome-wide autozygosity in Daghestan South Asian Sub 98 G=0.88 A=0.12
Genome-wide autozygosity in Daghestan Caucasus Sub 36 G=0.81 A=0.19
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.795 A=0.205
Northern Sweden ACPOP Study-wide 600 G=0.773 A=0.227
Qatari Global Study-wide 216 G=0.884 A=0.116
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.811 A=0.189
SGDP_PRJ Global Study-wide 166 G=0.452 A=0.542, T=0.006
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 70 G=0.94 A=0.06
The Danish reference pan genome Danish Study-wide 40 G=0.82 A=0.17
Siberian Global Study-wide 22 G=0.41 A=0.59
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 8 NC_000008.11:g.127391642G>A
GRCh38.p14 chr 8 NC_000008.11:g.127391642G>T
GRCh37.p13 chr 8 NC_000008.10:g.128403887G>A
GRCh37.p13 chr 8 NC_000008.10:g.128403887G>T
Gene: CASC21, cancer susceptibility 21 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
CASC21 transcript NR_117099.1:n. N/A Intron Variant
Gene: CASC8, cancer susceptibility 8 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CASC8 transcript variant 1 NR_117100.1:n. N/A Intron Variant
CASC8 transcript variant 2 NR_024393.1: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 G= A T
GRCh38.p14 chr 8 NC_000008.11:g.127391642= NC_000008.11:g.127391642G>A NC_000008.11:g.127391642G>T
GRCh37.p13 chr 8 NC_000008.10:g.128403887= NC_000008.10:g.128403887G>A NC_000008.10:g.128403887G>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#.

99 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss17219674 Feb 27, 2004 (120)
2 SC_SNP ss19015371 Feb 27, 2004 (120)
3 PERLEGEN ss24546094 Sep 20, 2004 (123)
4 ILLUMINA ss66732165 Nov 29, 2006 (127)
5 ILLUMINA ss66912665 Nov 29, 2006 (127)
6 ILLUMINA ss67046682 Nov 29, 2006 (127)
7 PERLEGEN ss69062060 May 16, 2007 (127)
8 ILLUMINA ss70386003 May 16, 2007 (127)
9 ILLUMINA ss70510297 May 25, 2008 (130)
10 ILLUMINA ss71037557 May 16, 2007 (127)
11 ILLUMINA ss75727760 Dec 06, 2007 (129)
12 KRIBB_YJKIM ss85040243 Dec 15, 2007 (130)
13 SNP500CANCER ss105437996 Feb 06, 2009 (130)
14 1000GENOMES ss108389934 Jan 23, 2009 (130)
15 SNP500CANCER ss120035118 Dec 01, 2009 (131)
16 ILLUMINA ss121424917 Dec 01, 2009 (131)
17 ILLUMINA ss152888644 Dec 01, 2009 (131)
18 ILLUMINA ss159155589 Dec 01, 2009 (131)
19 ILLUMINA ss159942988 Dec 01, 2009 (131)
20 ENSEMBL ss161608369 Dec 01, 2009 (131)
21 COMPLETE_GENOMICS ss162786861 Jul 04, 2010 (132)
22 ILLUMINA ss169732744 Jul 04, 2010 (132)
23 ILLUMINA ss170806819 Jul 04, 2010 (132)
24 1000GENOMES ss223978698 Jul 14, 2010 (132)
25 1000GENOMES ss234627288 Jul 15, 2010 (132)
26 1000GENOMES ss241441332 Jul 15, 2010 (132)
27 GMI ss285924798 Apr 25, 2013 (138)
28 ILLUMINA ss479837946 Sep 08, 2015 (146)
29 ILLUMINA ss483429914 May 04, 2012 (137)
30 ILLUMINA ss485541177 May 04, 2012 (137)
31 ILLUMINA ss535640612 Sep 08, 2015 (146)
32 TISHKOFF ss561069584 Apr 25, 2013 (138)
33 SSMP ss655503974 Apr 25, 2013 (138)
34 ILLUMINA ss780274256 Sep 08, 2015 (146)
35 ILLUMINA ss782158233 Sep 08, 2015 (146)
36 ILLUMINA ss825355436 Apr 01, 2015 (144)
37 ILLUMINA ss832668197 Jul 13, 2019 (153)
38 ILLUMINA ss835760391 Sep 08, 2015 (146)
39 EVA-GONL ss986056333 Aug 21, 2014 (142)
40 JMKIDD_LAB ss1075916639 Aug 21, 2014 (142)
41 1000GENOMES ss1331909632 Aug 21, 2014 (142)
42 HAMMER_LAB ss1397539571 Sep 08, 2015 (146)
43 DDI ss1431670529 Apr 01, 2015 (144)
44 EVA_GENOME_DK ss1582885404 Apr 01, 2015 (144)
45 EVA_DECODE ss1595672680 Apr 01, 2015 (144)
46 EVA_UK10K_ALSPAC ss1621728438 Apr 01, 2015 (144)
47 EVA_UK10K_TWINSUK ss1664722471 Apr 01, 2015 (144)
48 EVA_SVP ss1713070948 Apr 01, 2015 (144)
49 WEILL_CORNELL_DGM ss1929329306 Feb 12, 2016 (147)
50 ILLUMINA ss1959143053 Feb 12, 2016 (147)
51 JJLAB ss2025368118 Sep 14, 2016 (149)
52 USC_VALOUEV ss2153596789 Dec 20, 2016 (150)
53 HUMAN_LONGEVITY ss2307373864 Dec 20, 2016 (150)
54 ILLUMINA ss2634803760 Nov 08, 2017 (151)
55 ILLUMINA ss2635188347 Nov 08, 2017 (151)
56 GRF ss2709383750 Nov 08, 2017 (151)
57 ILLUMINA ss2711149498 Nov 08, 2017 (151)
58 GNOMAD ss2872694156 Nov 08, 2017 (151)
59 SWEGEN ss3003997327 Nov 08, 2017 (151)
60 ILLUMINA ss3022883346 Nov 08, 2017 (151)
61 BIOINF_KMB_FNS_UNIBA ss3026469689 Nov 08, 2017 (151)
62 CSHL ss3348404611 Nov 08, 2017 (151)
63 ILLUMINA ss3630158645 Oct 12, 2018 (152)
64 ILLUMINA ss3632699932 Oct 12, 2018 (152)
65 ILLUMINA ss3636932423 Oct 12, 2018 (152)
66 ILLUMINA ss3638786179 Oct 12, 2018 (152)
67 ILLUMINA ss3639396010 Oct 12, 2018 (152)
68 ILLUMINA ss3639729060 Oct 12, 2018 (152)
69 ILLUMINA ss3642658370 Oct 12, 2018 (152)
70 ILLUMINA ss3643715274 Oct 12, 2018 (152)
71 ILLUMINA ss3653429839 Oct 12, 2018 (152)
72 EGCUT_WGS ss3671720240 Jul 13, 2019 (153)
73 EVA_DECODE ss3723006013 Jul 13, 2019 (153)
74 ILLUMINA ss3726572161 Jul 13, 2019 (153)
75 ACPOP ss3736100515 Jul 13, 2019 (153)
76 EVA ss3768607296 Jul 13, 2019 (153)
77 PAGE_CC ss3771469331 Jul 13, 2019 (153)
78 KHV_HUMAN_GENOMES ss3811773521 Jul 13, 2019 (153)
79 EVA ss3831414376 Apr 26, 2020 (154)
80 HGDP ss3847929950 Apr 26, 2020 (154)
81 SGDP_PRJ ss3870994041 Apr 26, 2020 (154)
82 KRGDB ss3918595202 Apr 26, 2020 (154)
83 EVA ss3985389032 Apr 26, 2021 (155)
84 TOPMED ss4804204474 Apr 26, 2021 (155)
85 TOPMED ss4804204475 Apr 26, 2021 (155)
86 TOMMO_GENOMICS ss5190996650 Apr 26, 2021 (155)
87 1000G_HIGH_COVERAGE ss5278940254 Oct 16, 2022 (156)
88 EVA ss5315363794 Oct 16, 2022 (156)
89 EVA ss5384454346 Oct 16, 2022 (156)
90 HUGCELL_USP ss5475322175 Oct 16, 2022 (156)
91 HUGCELL_USP ss5475322176 Oct 16, 2022 (156)
92 1000G_HIGH_COVERAGE ss5570270562 Oct 16, 2022 (156)
93 SANFORD_IMAGENETICS ss5646413179 Oct 16, 2022 (156)
94 TOMMO_GENOMICS ss5733720400 Oct 16, 2022 (156)
95 YY_MCH ss5810133442 Oct 16, 2022 (156)
96 EVA ss5831223326 Oct 16, 2022 (156)
97 EVA ss5856572053 Oct 16, 2022 (156)
98 EVA ss5891026952 Oct 16, 2022 (156)
99 EVA ss5975664731 Oct 16, 2022 (156)
100 1000Genomes NC_000008.10 - 128403887 Oct 12, 2018 (152)
101 1000Genomes_30x NC_000008.11 - 127391642 Oct 16, 2022 (156)
102 The Avon Longitudinal Study of Parents and Children NC_000008.10 - 128403887 Oct 12, 2018 (152)
103 Genome-wide autozygosity in Daghestan NC_000008.9 - 128473069 Apr 26, 2020 (154)
104 Genetic variation in the Estonian population NC_000008.10 - 128403887 Oct 12, 2018 (152)
105 The Danish reference pan genome NC_000008.10 - 128403887 Apr 26, 2020 (154)
106 gnomAD - Genomes NC_000008.11 - 127391642 Apr 26, 2021 (155)
107 Genome of the Netherlands Release 5 NC_000008.10 - 128403887 Apr 26, 2020 (154)
108 HGDP-CEPH-db Supplement 1 NC_000008.9 - 128473069 Apr 26, 2020 (154)
109 HapMap NC_000008.11 - 127391642 Apr 26, 2020 (154)
110 KOREAN population from KRGDB NC_000008.10 - 128403887 Apr 26, 2020 (154)
111 Northern Sweden NC_000008.10 - 128403887 Jul 13, 2019 (153)
112 The PAGE Study NC_000008.11 - 127391642 Jul 13, 2019 (153)
113 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000008.10 - 128403887 Apr 26, 2021 (155)
114 Qatari NC_000008.10 - 128403887 Apr 26, 2020 (154)
115 SGDP_PRJ NC_000008.10 - 128403887 Apr 26, 2020 (154)
116 Siberian NC_000008.10 - 128403887 Apr 26, 2020 (154)
117 8.3KJPN NC_000008.10 - 128403887 Apr 26, 2021 (155)
118 14KJPN NC_000008.11 - 127391642 Oct 16, 2022 (156)
119 TopMed

Submission ignored due to conflicting rows:
Row 641582034 (NC_000008.11:127391641:G:A 35634/264690)
Row 641582035 (NC_000008.11:127391641:G:T 1/264690)

- Apr 26, 2021 (155)
120 TopMed

Submission ignored due to conflicting rows:
Row 641582034 (NC_000008.11:127391641:G:A 35634/264690)
Row 641582035 (NC_000008.11:127391641:G:T 1/264690)

- Apr 26, 2021 (155)
121 UK 10K study - Twins NC_000008.10 - 128403887 Oct 12, 2018 (152)
122 A Vietnamese Genetic Variation Database NC_000008.10 - 128403887 Jul 13, 2019 (153)
123 ALFA NC_000008.11 - 127391642 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)
rs17381907 Oct 08, 2004 (123)
rs60216223 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
513209, 607842, ss108389934, ss162786861, ss285924798, ss485541177, ss825355436, ss1397539571, ss1595672680, ss1713070948, ss2635188347, ss3639396010, ss3639729060, ss3643715274, ss3847929950 NC_000008.9:128473068:G:A NC_000008.11:127391641:G:A (self)
44109041, 24542650, 17458488, 9050341, 10952118, 25772596, 9385380, 614959, 11371236, 23011021, 6113143, 48965957, 24542650, 5451781, ss223978698, ss234627288, ss241441332, ss479837946, ss483429914, ss535640612, ss561069584, ss655503974, ss780274256, ss782158233, ss832668197, ss835760391, ss986056333, ss1075916639, ss1331909632, ss1431670529, ss1582885404, ss1621728438, ss1664722471, ss1929329306, ss1959143053, ss2025368118, ss2153596789, ss2634803760, ss2709383750, ss2711149498, ss2872694156, ss3003997327, ss3022883346, ss3348404611, ss3630158645, ss3632699932, ss3636932423, ss3638786179, ss3642658370, ss3653429839, ss3671720240, ss3736100515, ss3768607296, ss3831414376, ss3870994041, ss3918595202, ss3985389032, ss5190996650, ss5315363794, ss5384454346, ss5646413179, ss5831223326, ss5975664731 NC_000008.10:128403886:G:A NC_000008.11:127391641:G:A (self)
57796497, 311145617, 3724755, 690800, 67557504, 13819712924, ss2307373864, ss3026469689, ss3723006013, ss3726572161, ss3771469331, ss3811773521, ss4804204474, ss5278940254, ss5475322175, ss5570270562, ss5733720400, ss5810133442, ss5856572053, ss5891026952 NC_000008.11:127391641:G:A NC_000008.11:127391641:G:A (self)
ss17219674, ss19015371 NT_008046.14:41622065:G:A NC_000008.11:127391641:G:A (self)
ss24546094, ss66732165, ss66912665, ss67046682, ss69062060, ss70386003, ss70510297, ss71037557, ss75727760, ss85040243, ss105437996, ss120035118, ss121424917, ss152888644, ss159155589, ss159942988, ss161608369, ss169732744, ss170806819 NT_008046.16:41677435:G:A NC_000008.11:127391641:G:A (self)
23011021, ss3870994041 NC_000008.10:128403886:G:T NC_000008.11:127391641:G:T (self)
13819712924, ss2307373864, ss4804204475, ss5475322176 NC_000008.11:127391641:G:T NC_000008.11:127391641: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.

2 citations for rs10956365
PMID Title Author Year Journal
20699374 Evaluation of breast cancer susceptibility loci in Chinese women. Long J et al. 2010 Cancer epidemiology, biomarkers & prevention
25025429 Single nucleotide polymorphisms with cis-regulatory effects on long non-coding transcripts in human primary monocytes. Almlöf JC et al. 2014 PloS one
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