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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.

rs11150110

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr16:78897782 (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
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.341830 (90479/264690, TOPMED)
T=0.417111 (87862/210644, ALFA)
T=0.332933 (46598/139962, GnomAD) (+ 20 more)
T=0.25419 (7183/28258, 14KJPN)
T=0.25597 (4290/16760, 8.3KJPN)
T=0.3602 (2307/6404, 1000G_30x)
T=0.3636 (1821/5008, 1000G)
T=0.3748 (1679/4480, Estonian)
T=0.4144 (1597/3854, ALSPAC)
T=0.4215 (1563/3708, TWINSUK)
T=0.2802 (821/2930, KOREAN)
T=0.3905 (813/2082, HGDP_Stanford)
T=0.3344 (626/1872, HapMap)
T=0.2746 (503/1832, Korea1K)
T=0.395 (394/998, GoNL)
T=0.460 (288/626, Chileans)
T=0.307 (184/600, NorthernSweden)
C=0.355 (110/310, SGDP_PRJ)
C=0.458 (99/216, Qatari)
T=0.363 (77/212, Vietnamese)
T=0.28 (11/40, GENOME_DK)
C=0.42 (16/38, Ancient Sardinia)
C=0.37 (11/30, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
WWOX : 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 210644 C=0.582889 T=0.417111
European Sub 176990 C=0.573620 T=0.426380
African Sub 10410 C=0.82440 T=0.17560
African Others Sub 360 C=0.864 T=0.136
African American Sub 10050 C=0.82299 T=0.17701
Asian Sub 752 C=0.641 T=0.359
East Asian Sub 574 C=0.683 T=0.317
Other Asian Sub 178 C=0.506 T=0.494
Latin American 1 Sub 982 C=0.601 T=0.399
Latin American 2 Sub 9036 C=0.5504 T=0.4496
South Asian Sub 5050 C=0.4501 T=0.5499
Other Sub 7424 C=0.5869 T=0.4131


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 C=0.658170 T=0.341830
Allele Frequency Aggregator Total Global 210644 C=0.582889 T=0.417111
Allele Frequency Aggregator European Sub 176990 C=0.573620 T=0.426380
Allele Frequency Aggregator African Sub 10410 C=0.82440 T=0.17560
Allele Frequency Aggregator Latin American 2 Sub 9036 C=0.5504 T=0.4496
Allele Frequency Aggregator Other Sub 7424 C=0.5869 T=0.4131
Allele Frequency Aggregator South Asian Sub 5050 C=0.4501 T=0.5499
Allele Frequency Aggregator Latin American 1 Sub 982 C=0.601 T=0.399
Allele Frequency Aggregator Asian Sub 752 C=0.641 T=0.359
gnomAD - Genomes Global Study-wide 139962 C=0.667067 T=0.332933
gnomAD - Genomes European Sub 75800 C=0.60538 T=0.39462
gnomAD - Genomes African Sub 41962 C=0.83051 T=0.16949
gnomAD - Genomes American Sub 13610 C=0.55415 T=0.44585
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=0.4970 T=0.5030
gnomAD - Genomes East Asian Sub 3118 C=0.6790 T=0.3210
gnomAD - Genomes Other Sub 2148 C=0.6122 T=0.3878
14KJPN JAPANESE Study-wide 28258 C=0.74581 T=0.25419
8.3KJPN JAPANESE Study-wide 16760 C=0.74403 T=0.25597
1000Genomes_30x Global Study-wide 6404 C=0.6398 T=0.3602
1000Genomes_30x African Sub 1786 C=0.8841 T=0.1159
1000Genomes_30x Europe Sub 1266 C=0.5411 T=0.4589
1000Genomes_30x South Asian Sub 1202 C=0.4268 T=0.5732
1000Genomes_30x East Asian Sub 1170 C=0.6769 T=0.3231
1000Genomes_30x American Sub 980 C=0.539 T=0.461
1000Genomes Global Study-wide 5008 C=0.6364 T=0.3636
1000Genomes African Sub 1322 C=0.8752 T=0.1248
1000Genomes East Asian Sub 1008 C=0.6776 T=0.3224
1000Genomes Europe Sub 1006 C=0.5547 T=0.4453
1000Genomes South Asian Sub 978 C=0.417 T=0.583
1000Genomes American Sub 694 C=0.549 T=0.451
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.6252 T=0.3748
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.5856 T=0.4144
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.5785 T=0.4215
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.7198 T=0.2802
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 C=0.6095 T=0.3905
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 C=0.687 T=0.313
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.478 T=0.522
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.483 T=0.517
HGDP-CEPH-db Supplement 1 Europe Sub 320 C=0.544 T=0.456
HGDP-CEPH-db Supplement 1 Africa Sub 240 C=0.933 T=0.067
HGDP-CEPH-db Supplement 1 America Sub 216 C=0.574 T=0.426
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=0.79 T=0.21
HapMap Global Study-wide 1872 C=0.6656 T=0.3344
HapMap American Sub 760 C=0.557 T=0.443
HapMap African Sub 682 C=0.804 T=0.196
HapMap Asian Sub 254 C=0.705 T=0.295
HapMap Europe Sub 176 C=0.545 T=0.455
Korean Genome Project KOREAN Study-wide 1832 C=0.7254 T=0.2746
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.605 T=0.395
Chileans Chilean Study-wide 626 C=0.540 T=0.460
Northern Sweden ACPOP Study-wide 600 C=0.693 T=0.307
SGDP_PRJ Global Study-wide 310 C=0.355 T=0.645
Qatari Global Study-wide 216 C=0.458 T=0.542
A Vietnamese Genetic Variation Database Global Study-wide 212 C=0.637 T=0.363
The Danish reference pan genome Danish Study-wide 40 C=0.72 T=0.28
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 38 C=0.42 T=0.58
Siberian Global Study-wide 30 C=0.37 T=0.63
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 16 NC_000016.10:g.78897782C>T
GRCh37.p13 chr 16 NC_000016.9:g.78931679C>T
WWOX RefSeqGene NG_011698.1:g.803129C>T
Gene: WWOX, WW domain containing oxidoreductase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
WWOX transcript variant 4 NM_001291997.2:c.718-3138…

NM_001291997.2:c.718-313826C>T

N/A Intron Variant
WWOX transcript variant 1 NM_016373.4:c.1057-313826…

NM_016373.4:c.1057-313826C>T

N/A Intron Variant
WWOX transcript variant 2 NM_130791.5:c. N/A Genic Downstream Transcript Variant
WWOX transcript variant 3 NR_120435.2:n. N/A Genic Downstream Transcript Variant
WWOX transcript variant 5 NR_120436.3: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 C= T
GRCh38.p14 chr 16 NC_000016.10:g.78897782= NC_000016.10:g.78897782C>T
GRCh37.p13 chr 16 NC_000016.9:g.78931679= NC_000016.9:g.78931679C>T
WWOX RefSeqGene NG_011698.1:g.803129= NG_011698.1:g.803129C>T
WWOX transcript variant 4 NM_001291997.2:c.718-313826= NM_001291997.2:c.718-313826C>T
WWOX transcript variant 1 NM_016373.2:c.1057-313826= NM_016373.2:c.1057-313826C>T
WWOX transcript variant 1 NM_016373.4:c.1057-313826= NM_016373.4:c.1057-313826C>T
WWOX transcript variant X1 XM_005255980.1:c.410-313826= XM_005255980.1:c.410-313826C>T
WWOX transcript variant X2 XM_005255981.1:c.718-313826= XM_005255981.1:c.718-313826C>T
WWOX transcript variant X3 XM_005255982.1:c.517-313826= XM_005255982.1:c.517-313826C>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#.

114 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss16700091 Feb 27, 2004 (120)
2 CSHL-HAPMAP ss19336342 Feb 27, 2004 (120)
3 SSAHASNP ss21321120 Apr 05, 2004 (121)
4 ABI ss40721840 Mar 14, 2006 (126)
5 ILLUMINA ss66795203 Nov 29, 2006 (127)
6 ILLUMINA ss66923703 Nov 29, 2006 (127)
7 ILLUMINA ss67072496 Nov 29, 2006 (127)
8 ILLUMINA ss70390796 May 16, 2007 (127)
9 ILLUMINA ss70521563 May 25, 2008 (130)
10 ILLUMINA ss71050675 May 16, 2007 (127)
11 ILLUMINA ss75824148 Dec 06, 2007 (129)
12 AFFY ss76456282 Dec 06, 2007 (129)
13 HGSV ss82269527 Dec 15, 2007 (130)
14 KRIBB_YJKIM ss85077641 Dec 15, 2007 (130)
15 HUMANGENOME_JCVI ss96717301 Feb 13, 2009 (130)
16 1000GENOMES ss109473380 Jan 24, 2009 (130)
17 ILLUMINA ss121453125 Dec 01, 2009 (131)
18 ENSEMBL ss136671514 Dec 01, 2009 (131)
19 ILLUMINA ss152947551 Dec 01, 2009 (131)
20 ILLUMINA ss159167267 Dec 01, 2009 (131)
21 ILLUMINA ss159963503 Dec 01, 2009 (131)
22 COMPLETE_GENOMICS ss168518876 Jul 04, 2010 (132)
23 ILLUMINA ss169807070 Jul 04, 2010 (132)
24 ILLUMINA ss171091614 Jul 04, 2010 (132)
25 1000GENOMES ss227346169 Jul 14, 2010 (132)
26 1000GENOMES ss237100094 Jul 15, 2010 (132)
27 1000GENOMES ss243425600 Jul 15, 2010 (132)
28 BL ss255826624 May 09, 2011 (134)
29 GMI ss282609641 May 04, 2012 (137)
30 GMI ss287109148 Apr 25, 2013 (138)
31 PJP ss291880592 May 09, 2011 (134)
32 ILLUMINA ss479479083 May 04, 2012 (137)
33 ILLUMINA ss479483088 May 04, 2012 (137)
34 ILLUMINA ss479919778 Sep 08, 2015 (146)
35 ILLUMINA ss484539133 May 04, 2012 (137)
36 ILLUMINA ss536679990 Sep 08, 2015 (146)
37 TISHKOFF ss565026107 Apr 25, 2013 (138)
38 ILLUMINA ss778754070 Sep 08, 2015 (146)
39 ILLUMINA ss782716197 Sep 08, 2015 (146)
40 ILLUMINA ss783683863 Sep 08, 2015 (146)
41 ILLUMINA ss825360191 Apr 01, 2015 (144)
42 ILLUMINA ss831967651 Sep 08, 2015 (146)
43 ILLUMINA ss832679822 Jul 13, 2019 (153)
44 ILLUMINA ss834213766 Sep 08, 2015 (146)
45 EVA-GONL ss992701815 Aug 21, 2014 (142)
46 JMKIDD_LAB ss1080774015 Aug 21, 2014 (142)
47 1000GENOMES ss1357061072 Aug 21, 2014 (142)
48 DDI ss1427905401 Apr 01, 2015 (144)
49 EVA_GENOME_DK ss1577997484 Apr 01, 2015 (144)
50 EVA_UK10K_ALSPAC ss1634857589 Apr 01, 2015 (144)
51 EVA_UK10K_TWINSUK ss1677851622 Apr 01, 2015 (144)
52 EVA_SVP ss1713553635 Apr 01, 2015 (144)
53 ILLUMINA ss1752205466 Sep 08, 2015 (146)
54 HAMMER_LAB ss1808601687 Sep 08, 2015 (146)
55 WEILL_CORNELL_DGM ss1936132652 Feb 12, 2016 (147)
56 GENOMED ss1968305822 Jul 19, 2016 (147)
57 JJLAB ss2028853564 Sep 14, 2016 (149)
58 USC_VALOUEV ss2157294349 Dec 20, 2016 (150)
59 HUMAN_LONGEVITY ss2213841404 Dec 20, 2016 (150)
60 SYSTEMSBIOZJU ss2628918479 Nov 08, 2017 (151)
61 ILLUMINA ss2633343364 Nov 08, 2017 (151)
62 ILLUMINA ss2635065956 Nov 08, 2017 (151)
63 GRF ss2701827136 Nov 08, 2017 (151)
64 GNOMAD ss2945367559 Nov 08, 2017 (151)
65 SWEGEN ss3014847944 Nov 08, 2017 (151)
66 BIOINF_KMB_FNS_UNIBA ss3028243648 Nov 08, 2017 (151)
67 CSHL ss3351544348 Nov 08, 2017 (151)
68 ILLUMINA ss3627570199 Oct 12, 2018 (152)
69 ILLUMINA ss3631328125 Oct 12, 2018 (152)
70 ILLUMINA ss3633127216 Oct 12, 2018 (152)
71 ILLUMINA ss3633833644 Oct 12, 2018 (152)
72 ILLUMINA ss3634651661 Oct 12, 2018 (152)
73 ILLUMINA ss3635521796 Oct 12, 2018 (152)
74 ILLUMINA ss3636343028 Oct 12, 2018 (152)
75 ILLUMINA ss3637273260 Oct 12, 2018 (152)
76 ILLUMINA ss3638136599 Oct 12, 2018 (152)
77 ILLUMINA ss3639079090 Oct 12, 2018 (152)
78 ILLUMINA ss3639546059 Oct 12, 2018 (152)
79 ILLUMINA ss3640358981 Oct 12, 2018 (152)
80 ILLUMINA ss3643116902 Oct 12, 2018 (152)
81 URBANLAB ss3650551857 Oct 12, 2018 (152)
82 EGCUT_WGS ss3681826037 Jul 13, 2019 (153)
83 EVA_DECODE ss3699665407 Jul 13, 2019 (153)
84 ACPOP ss3741684495 Jul 13, 2019 (153)
85 ILLUMINA ss3744952078 Jul 13, 2019 (153)
86 EVA ss3754182720 Jul 13, 2019 (153)
87 ILLUMINA ss3772450251 Jul 13, 2019 (153)
88 PACBIO ss3788092945 Jul 13, 2019 (153)
89 PACBIO ss3793066395 Jul 13, 2019 (153)
90 PACBIO ss3797951525 Jul 13, 2019 (153)
91 KHV_HUMAN_GENOMES ss3819462388 Jul 13, 2019 (153)
92 EVA ss3834669374 Apr 27, 2020 (154)
93 EVA ss3840940500 Apr 27, 2020 (154)
94 EVA ss3846433406 Apr 27, 2020 (154)
95 HGDP ss3847551328 Apr 27, 2020 (154)
96 SGDP_PRJ ss3884868302 Apr 27, 2020 (154)
97 KRGDB ss3934411559 Apr 27, 2020 (154)
98 KOGIC ss3977988515 Apr 27, 2020 (154)
99 EVA ss3985768224 Apr 27, 2021 (155)
100 EVA ss4017746153 Apr 27, 2021 (155)
101 TOPMED ss5022601577 Apr 27, 2021 (155)
102 TOMMO_GENOMICS ss5220523979 Apr 27, 2021 (155)
103 1000G_HIGH_COVERAGE ss5301675845 Oct 17, 2022 (156)
104 EVA ss5315852774 Oct 17, 2022 (156)
105 EVA ss5425035245 Oct 17, 2022 (156)
106 HUGCELL_USP ss5494948137 Oct 17, 2022 (156)
107 1000G_HIGH_COVERAGE ss5604699953 Oct 17, 2022 (156)
108 SANFORD_IMAGENETICS ss5659299505 Oct 17, 2022 (156)
109 TOMMO_GENOMICS ss5775812079 Oct 17, 2022 (156)
110 YY_MCH ss5816145315 Oct 17, 2022 (156)
111 EVA ss5846688522 Oct 17, 2022 (156)
112 EVA ss5851648222 Oct 17, 2022 (156)
113 EVA ss5899907338 Oct 17, 2022 (156)
114 EVA ss5950706314 Oct 17, 2022 (156)
115 1000Genomes NC_000016.9 - 78931679 Oct 12, 2018 (152)
116 1000Genomes_30x NC_000016.10 - 78897782 Oct 17, 2022 (156)
117 The Avon Longitudinal Study of Parents and Children NC_000016.9 - 78931679 Oct 12, 2018 (152)
118 Chileans NC_000016.9 - 78931679 Apr 27, 2020 (154)
119 Genetic variation in the Estonian population NC_000016.9 - 78931679 Oct 12, 2018 (152)
120 The Danish reference pan genome NC_000016.9 - 78931679 Apr 27, 2020 (154)
121 gnomAD - Genomes NC_000016.10 - 78897782 Apr 27, 2021 (155)
122 Genome of the Netherlands Release 5 NC_000016.9 - 78931679 Apr 27, 2020 (154)
123 HGDP-CEPH-db Supplement 1 NC_000016.8 - 77489180 Apr 27, 2020 (154)
124 HapMap NC_000016.10 - 78897782 Apr 27, 2020 (154)
125 KOREAN population from KRGDB NC_000016.9 - 78931679 Apr 27, 2020 (154)
126 Korean Genome Project NC_000016.10 - 78897782 Apr 27, 2020 (154)
127 Northern Sweden NC_000016.9 - 78931679 Jul 13, 2019 (153)
128 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000016.9 - 78931679 Apr 27, 2021 (155)
129 Qatari NC_000016.9 - 78931679 Apr 27, 2020 (154)
130 SGDP_PRJ NC_000016.9 - 78931679 Apr 27, 2020 (154)
131 Siberian NC_000016.9 - 78931679 Apr 27, 2020 (154)
132 8.3KJPN NC_000016.9 - 78931679 Apr 27, 2021 (155)
133 14KJPN NC_000016.10 - 78897782 Oct 17, 2022 (156)
134 TopMed NC_000016.10 - 78897782 Apr 27, 2021 (155)
135 UK 10K study - Twins NC_000016.9 - 78931679 Oct 12, 2018 (152)
136 A Vietnamese Genetic Variation Database NC_000016.9 - 78931679 Jul 13, 2019 (153)
137 ALFA NC_000016.10 - 78897782 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)
rs59925876 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
229220, ss76456282, ss82269527, ss109473380, ss168518876, ss255826624, ss282609641, ss287109148, ss291880592, ss479479083, ss825360191, ss1713553635, ss2635065956, ss3639079090, ss3639546059, ss3643116902, ss3847551328 NC_000016.8:77489179:C:T NC_000016.10:78897781:C:T (self)
70250889, 38974876, 172834, 27564285, 4206454, 17375339, 41588953, 14969360, 994151, 18174574, 36885282, 9810703, 78493286, 38974876, 8638522, ss227346169, ss237100094, ss243425600, ss479483088, ss479919778, ss484539133, ss536679990, ss565026107, ss778754070, ss782716197, ss783683863, ss831967651, ss832679822, ss834213766, ss992701815, ss1080774015, ss1357061072, ss1427905401, ss1577997484, ss1634857589, ss1677851622, ss1752205466, ss1808601687, ss1936132652, ss1968305822, ss2028853564, ss2157294349, ss2628918479, ss2633343364, ss2701827136, ss2945367559, ss3014847944, ss3351544348, ss3627570199, ss3631328125, ss3633127216, ss3633833644, ss3634651661, ss3635521796, ss3636343028, ss3637273260, ss3638136599, ss3640358981, ss3681826037, ss3741684495, ss3744952078, ss3754182720, ss3772450251, ss3788092945, ss3793066395, ss3797951525, ss3834669374, ss3840940500, ss3884868302, ss3934411559, ss3985768224, ss4017746153, ss5220523979, ss5315852774, ss5425035245, ss5659299505, ss5846688522, ss5950706314 NC_000016.9:78931678:C:T NC_000016.10:78897781:C:T (self)
92225888, 495611563, 1419983, 34366516, 109649183, 238147238, 9015944329, ss2213841404, ss3028243648, ss3650551857, ss3699665407, ss3819462388, ss3846433406, ss3977988515, ss5022601577, ss5301675845, ss5494948137, ss5604699953, ss5775812079, ss5816145315, ss5851648222, ss5899907338 NC_000016.10:78897781:C:T NC_000016.10:78897781:C:T (self)
ss96717301 NT_010498.15:32545871:AACCCCC:AACC…

NT_010498.15:32545871:AACCCCC:AACCCCT

NC_000016.10:78897781:C:T (self)
ss40721840, ss66795203, ss66923703, ss67072496, ss70390796, ss70521563, ss71050675, ss75824148, ss85077641, ss121453125, ss136671514, ss152947551, ss159167267, ss159963503, ss169807070, ss171091614 NT_010498.15:32545877:C:T NC_000016.10:78897781:C:T (self)
ss16700091, ss19336342, ss21321120 NT_024797.14:5643365:C:T NC_000016.10:78897781:C: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 rs11150110

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