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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.

rs10833965

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr11:23193334 (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
A>C / A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.412612 (111015/269054, ALFA)
A=0.424387 (112331/264690, TOPMED)
A=0.38700 (30457/78700, PAGE_STUDY) (+ 19 more)
A=0.00024 (4/16758, 8.3KJPN)
A=0.3417 (1711/5008, 1000G)
A=0.4460 (1998/4480, Estonian)
A=0.4024 (1551/3854, ALSPAC)
A=0.3959 (1468/3708, TWINSUK)
A=0.0024 (7/2930, KOREAN)
A=0.3127 (651/2082, HGDP_Stanford)
A=0.0005 (1/1832, Korea1K)
A=0.3680 (666/1810, HapMap)
A=0.427 (426/998, GoNL)
A=0.009 (7/792, PRJEB37584)
A=0.460 (276/600, NorthernSweden)
A=0.189 (95/502, SGDP_PRJ)
A=0.500 (108/216, Qatari)
G=0.500 (108/216, Qatari)
A=0.038 (8/212, Vietnamese)
A=0.18 (9/50, Siberian)
A=0.40 (16/40, GENOME_DK)
A=0.42 (10/24, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LINC02718 : 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 11 NC_000011.10:g.23193334A>C
GRCh38.p13 chr 11 NC_000011.10:g.23193334A>G
GRCh38.p13 chr 11 NC_000011.10:g.23193334A>T
GRCh37.p13 chr 11 NC_000011.9:g.23214880A>C
GRCh37.p13 chr 11 NC_000011.9:g.23214880A>G
GRCh37.p13 chr 11 NC_000011.9:g.23214880A>T
Gene: LINC02718, uncharacterized LINC02718 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LINC02718 transcript XR_001748156.2: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

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 269054 A=0.412612 C=0.000000, G=0.587388, T=0.000000
European Sub 242356 A=0.417233 C=0.000000, G=0.582767, T=0.000000
African Sub 6300 A=0.5694 C=0.0000, G=0.4306, T=0.0000
African Others Sub 258 A=0.640 C=0.000, G=0.360, T=0.000
African American Sub 6042 A=0.5664 C=0.0000, G=0.4336, T=0.0000
Asian Sub 3532 A=0.0113 C=0.0000, G=0.9887, T=0.0000
East Asian Sub 2846 A=0.0053 C=0.0000, G=0.9947, T=0.0000
Other Asian Sub 686 A=0.036 C=0.000, G=0.964, T=0.000
Latin American 1 Sub 924 A=0.484 C=0.000, G=0.516, T=0.000
Latin American 2 Sub 2442 A=0.3444 C=0.0000, G=0.6556, T=0.0000
South Asian Sub 5098 A=0.3423 C=0.0000, G=0.6577, T=0.0000
Other Sub 8402 A=0.3851 C=0.0000, G=0.6149, 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=0.424387 G=0.575613
The PAGE Study Global Study-wide 78700 A=0.38700 G=0.61300
The PAGE Study AfricanAmerican Sub 32514 A=0.52528 G=0.47472
The PAGE Study Mexican Sub 10810 A=0.30555 G=0.69445
The PAGE Study Asian Sub 8318 A=0.0057 G=0.9943
The PAGE Study PuertoRican Sub 7918 A=0.4033 G=0.5967
The PAGE Study NativeHawaiian Sub 4534 A=0.1641 G=0.8359
The PAGE Study Cuban Sub 4230 A=0.4461 G=0.5539
The PAGE Study Dominican Sub 3828 A=0.4723 G=0.5277
The PAGE Study CentralAmerican Sub 2450 A=0.3576 G=0.6424
The PAGE Study SouthAmerican Sub 1982 A=0.3860 G=0.6140
The PAGE Study NativeAmerican Sub 1260 A=0.3857 G=0.6143
The PAGE Study SouthAsian Sub 856 A=0.314 G=0.686
8.3KJPN JAPANESE Study-wide 16758 A=0.00024 G=0.99976
1000Genomes Global Study-wide 5008 A=0.3417 G=0.6583
1000Genomes African Sub 1322 A=0.5356 G=0.4644
1000Genomes East Asian Sub 1008 A=0.0179 G=0.9821
1000Genomes Europe Sub 1006 A=0.4026 G=0.5974
1000Genomes South Asian Sub 978 A=0.315 G=0.685
1000Genomes American Sub 694 A=0.392 G=0.608
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.4460 G=0.5540
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.4024 G=0.5976
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.3959 G=0.6041
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.0024 C=0.0000, G=0.9976
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 A=0.3127 G=0.6873
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.026 G=0.974
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.362 G=0.638
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.489 G=0.511
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.397 G=0.603
HGDP-CEPH-db Supplement 1 Africa Sub 240 A=0.646 G=0.354
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.139 G=0.861
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.08 G=0.92
Korean Genome Project KOREAN Study-wide 1832 A=0.0005 G=0.9995
HapMap Global Study-wide 1810 A=0.3680 G=0.6320
HapMap American Sub 770 A=0.304 G=0.696
HapMap African Sub 692 A=0.512 G=0.488
HapMap Europe Sub 176 A=0.438 G=0.562
HapMap Asian Sub 172 A=0.006 G=0.994
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.427 G=0.573
CNV burdens in cranial meningiomas Global Study-wide 792 A=0.009 G=0.991
CNV burdens in cranial meningiomas CRM Sub 792 A=0.009 G=0.991
Northern Sweden ACPOP Study-wide 600 A=0.460 G=0.540
SGDP_PRJ Global Study-wide 502 A=0.189 G=0.811
Qatari Global Study-wide 216 A=0.500 G=0.500
A Vietnamese Genetic Variation Database Global Study-wide 212 A=0.038 G=0.962
Siberian Global Study-wide 50 A=0.18 G=0.82
The Danish reference pan genome Danish Study-wide 40 A=0.40 G=0.60
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 24 A=0.42 G=0.58
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= C G T
GRCh38.p13 chr 11 NC_000011.10:g.23193334= NC_000011.10:g.23193334A>C NC_000011.10:g.23193334A>G NC_000011.10:g.23193334A>T
GRCh37.p13 chr 11 NC_000011.9:g.23214880= NC_000011.9:g.23214880A>C NC_000011.9:g.23214880A>G NC_000011.9:g.23214880A>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#.

123 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_SNP ss15603454 Feb 27, 2004 (120)
2 SC_SNP ss18468174 Feb 27, 2004 (120)
3 SC_SNP ss18693497 Feb 27, 2004 (120)
4 PERLEGEN ss23679664 Sep 20, 2004 (123)
5 ABI ss39958845 Mar 15, 2006 (126)
6 ILLUMINA ss66903706 Dec 01, 2006 (127)
7 ILLUMINA ss67026009 Dec 01, 2006 (127)
8 ILLUMINA ss68091195 Dec 12, 2006 (127)
9 ILLUMINA ss70501186 May 26, 2008 (130)
10 ILLUMINA ss71027134 May 18, 2007 (127)
11 ILLUMINA ss75766899 Dec 07, 2007 (129)
12 KRIBB_YJKIM ss85010657 Dec 15, 2007 (130)
13 HGSV ss85677418 Dec 15, 2007 (130)
14 BCMHGSC_JDW ss88502462 Mar 24, 2008 (129)
15 HUMANGENOME_JCVI ss97370689 Feb 06, 2009 (130)
16 BGI ss106727949 Feb 06, 2009 (130)
17 1000GENOMES ss110166910 Jan 24, 2009 (130)
18 1000GENOMES ss114336708 Jan 25, 2009 (130)
19 ILLUMINA-UK ss119733908 Dec 01, 2009 (131)
20 ENSEMBL ss132361237 Dec 01, 2009 (131)
21 ENSEMBL ss137775761 Dec 01, 2009 (131)
22 ILLUMINA ss152841137 Dec 01, 2009 (131)
23 GMI ss156043010 Dec 01, 2009 (131)
24 ILLUMINA ss159146200 Dec 01, 2009 (131)
25 ILLUMINA ss159927122 Dec 01, 2009 (131)
26 COMPLETE_GENOMICS ss169357840 Jul 04, 2010 (132)
27 ILLUMINA ss170611600 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss170658628 Jul 04, 2010 (132)
29 BUSHMAN ss202485888 Jul 04, 2010 (132)
30 BCM-HGSC-SUB ss207684977 Jul 04, 2010 (132)
31 1000GENOMES ss225142150 Jul 14, 2010 (132)
32 1000GENOMES ss235482833 Jul 15, 2010 (132)
33 1000GENOMES ss242130606 Jul 15, 2010 (132)
34 BL ss254967138 May 09, 2011 (134)
35 GMI ss280922090 May 04, 2012 (137)
36 GMI ss286334608 Apr 25, 2013 (138)
37 PJP ss291199215 May 09, 2011 (134)
38 ILLUMINA ss479369084 May 04, 2012 (137)
39 ILLUMINA ss479372229 May 04, 2012 (137)
40 ILLUMINA ss479774356 Sep 08, 2015 (146)
41 ILLUMINA ss484484680 May 04, 2012 (137)
42 ILLUMINA ss536641231 Sep 08, 2015 (146)
43 TISHKOFF ss562443411 Apr 25, 2013 (138)
44 SSMP ss657901972 Apr 25, 2013 (138)
45 ILLUMINA ss780668265 Aug 21, 2014 (142)
46 ILLUMINA ss782688879 Sep 08, 2015 (146)
47 ILLUMINA ss783657193 Aug 21, 2014 (142)
48 ILLUMINA ss831939809 Sep 08, 2015 (146)
49 ILLUMINA ss832658832 Jul 13, 2019 (153)
50 ILLUMINA ss836164130 Aug 21, 2014 (142)
51 EVA-GONL ss988304134 Aug 21, 2014 (142)
52 JMKIDD_LAB ss1077574232 Aug 21, 2014 (142)
53 1000GENOMES ss1340471654 Aug 21, 2014 (142)
54 DDI ss1426567549 Apr 01, 2015 (144)
55 EVA_GENOME_DK ss1575584398 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1626179189 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1669173222 Apr 01, 2015 (144)
58 EVA_SVP ss1713241538 Apr 01, 2015 (144)
59 ILLUMINA ss1752010257 Sep 08, 2015 (146)
60 HAMMER_LAB ss1806734211 Sep 08, 2015 (146)
61 WEILL_CORNELL_DGM ss1931666282 Feb 12, 2016 (147)
62 ILLUMINA ss1946305389 Feb 12, 2016 (147)
63 ILLUMINA ss1959333938 Feb 12, 2016 (147)
64 GENOMED ss1967317136 Jul 19, 2016 (147)
65 JJLAB ss2026578360 Sep 14, 2016 (149)
66 USC_VALOUEV ss2154867121 Dec 20, 2016 (150)
67 HUMAN_LONGEVITY ss2180909740 Dec 20, 2016 (150)
68 TOPMED ss2344080138 Dec 20, 2016 (150)
69 SYSTEMSBIOZJU ss2627761578 Nov 08, 2017 (151)
70 ILLUMINA ss2632813665 Nov 08, 2017 (151)
71 GRF ss2699143507 Nov 08, 2017 (151)
72 ILLUMINA ss2710731415 Nov 08, 2017 (151)
73 GNOMAD ss2897317304 Nov 08, 2017 (151)
74 SWEGEN ss3007741106 Nov 08, 2017 (151)
75 ILLUMINA ss3021318078 Nov 08, 2017 (151)
76 BIOINF_KMB_FNS_UNIBA ss3027086675 Nov 08, 2017 (151)
77 TOPMED ss3139324959 Nov 08, 2017 (151)
78 CSHL ss3349496949 Nov 08, 2017 (151)
79 ILLUMINA ss3625597911 Oct 12, 2018 (152)
80 ILLUMINA ss3626621135 Oct 12, 2018 (152)
81 ILLUMINA ss3630832255 Oct 12, 2018 (152)
82 ILLUMINA ss3632979527 Oct 12, 2018 (152)
83 ILLUMINA ss3633678414 Oct 12, 2018 (152)
84 ILLUMINA ss3634445862 Oct 12, 2018 (152)
85 ILLUMINA ss3635370208 Oct 12, 2018 (152)
86 ILLUMINA ss3636130133 Oct 12, 2018 (152)
87 ILLUMINA ss3637121030 Oct 12, 2018 (152)
88 ILLUMINA ss3637896730 Oct 12, 2018 (152)
89 ILLUMINA ss3638963760 Oct 12, 2018 (152)
90 ILLUMINA ss3639793115 Oct 12, 2018 (152)
91 ILLUMINA ss3640153201 Oct 12, 2018 (152)
92 ILLUMINA ss3641012892 Oct 12, 2018 (152)
93 ILLUMINA ss3641307294 Oct 12, 2018 (152)
94 ILLUMINA ss3642895965 Oct 12, 2018 (152)
95 ILLUMINA ss3643845373 Oct 12, 2018 (152)
96 ILLUMINA ss3644558193 Oct 12, 2018 (152)
97 URBANLAB ss3649556250 Oct 12, 2018 (152)
98 ILLUMINA ss3651680780 Oct 12, 2018 (152)
99 EGCUT_WGS ss3675142337 Jul 13, 2019 (153)
100 EVA_DECODE ss3691387362 Jul 13, 2019 (153)
101 ILLUMINA ss3725225429 Jul 13, 2019 (153)
102 ACPOP ss3737999715 Jul 13, 2019 (153)
103 ILLUMINA ss3744082332 Jul 13, 2019 (153)
104 ILLUMINA ss3744746764 Jul 13, 2019 (153)
105 EVA ss3749052973 Jul 13, 2019 (153)
106 PAGE_CC ss3771612876 Jul 13, 2019 (153)
107 ILLUMINA ss3772246798 Jul 13, 2019 (153)
108 PACBIO ss3786895165 Jul 13, 2019 (153)
109 PACBIO ss3792045090 Jul 13, 2019 (153)
110 PACBIO ss3796927179 Jul 13, 2019 (153)
111 KHV_HUMAN_GENOMES ss3814401252 Jul 13, 2019 (153)
112 EVA ss3832526520 Apr 26, 2020 (154)
113 EVA ss3839812495 Apr 26, 2020 (154)
114 EVA ss3845289502 Apr 26, 2020 (154)
115 HGDP ss3847413054 Apr 26, 2020 (154)
116 SGDP_PRJ ss3875831789 Apr 26, 2020 (154)
117 KRGDB ss3924076046 Apr 26, 2020 (154)
118 KOGIC ss3969380780 Apr 26, 2020 (154)
119 EVA ss3984647820 Apr 26, 2021 (155)
120 EVA ss3985524540 Apr 26, 2021 (155)
121 EVA ss4017528599 Apr 26, 2021 (155)
122 TOPMED ss4878254431 Apr 26, 2021 (155)
123 TOMMO_GENOMICS ss5201072883 Apr 26, 2021 (155)
124 1000Genomes NC_000011.9 - 23214880 Oct 12, 2018 (152)
125 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 23214880 Oct 12, 2018 (152)
126 Genetic variation in the Estonian population NC_000011.9 - 23214880 Oct 12, 2018 (152)
127 The Danish reference pan genome NC_000011.9 - 23214880 Apr 26, 2020 (154)
128 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 373864742 (NC_000011.10:23193333:A:C 0/139900)
Row 373864743 (NC_000011.10:23193333:A:G 78989/139818)

- Apr 26, 2021 (155)
129 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 373864742 (NC_000011.10:23193333:A:C 0/139900)
Row 373864743 (NC_000011.10:23193333:A:G 78989/139818)

- Apr 26, 2021 (155)
130 Genome of the Netherlands Release 5 NC_000011.9 - 23214880 Apr 26, 2020 (154)
131 HGDP-CEPH-db Supplement 1 NC_000011.8 - 23171456 Apr 26, 2020 (154)
132 HapMap NC_000011.10 - 23193334 Apr 26, 2020 (154)
133 KOREAN population from KRGDB NC_000011.9 - 23214880 Apr 26, 2020 (154)
134 Korean Genome Project NC_000011.10 - 23193334 Apr 26, 2020 (154)
135 Northern Sweden NC_000011.9 - 23214880 Jul 13, 2019 (153)
136 The PAGE Study NC_000011.10 - 23193334 Jul 13, 2019 (153)
137 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000011.9 - 23214880 Apr 26, 2021 (155)
138 CNV burdens in cranial meningiomas NC_000011.9 - 23214880 Apr 26, 2021 (155)
139 Qatari NC_000011.9 - 23214880 Apr 26, 2020 (154)
140 SGDP_PRJ NC_000011.9 - 23214880 Apr 26, 2020 (154)
141 Siberian NC_000011.9 - 23214880 Apr 26, 2020 (154)
142 8.3KJPN NC_000011.9 - 23214880 Apr 26, 2021 (155)
143 TopMed NC_000011.10 - 23193334 Apr 26, 2021 (155)
144 UK 10K study - Twins NC_000011.9 - 23214880 Oct 12, 2018 (152)
145 A Vietnamese Genetic Variation Database NC_000011.9 - 23214880 Jul 13, 2019 (153)
146 ALFA NC_000011.10 - 23193334 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)
rs60515807 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
31253440, ss3924076046 NC_000011.9:23214879:A:C NC_000011.10:23193333:A:C (self)
5054679372 NC_000011.10:23193333:A:C NC_000011.10:23193333:A:C
90946, ss85677418, ss88502462, ss110166910, ss114336708, ss119733908, ss169357840, ss170658628, ss202485888, ss207684977, ss254967138, ss280922090, ss286334608, ss291199215, ss479369084, ss1713241538, ss3638963760, ss3639793115, ss3642895965, ss3643845373, ss3847413054 NC_000011.8:23171455:A:G NC_000011.10:23193333:A:G (self)
52966904, 29423790, 20880585, 2482201, 13120786, 31253440, 11284580, 750467, 197295, 13708212, 27848769, 7383475, 59042190, 29423790, 6533977, ss225142150, ss235482833, ss242130606, ss479372229, ss479774356, ss484484680, ss536641231, ss562443411, ss657901972, ss780668265, ss782688879, ss783657193, ss831939809, ss832658832, ss836164130, ss988304134, ss1077574232, ss1340471654, ss1426567549, ss1575584398, ss1626179189, ss1669173222, ss1752010257, ss1806734211, ss1931666282, ss1946305389, ss1959333938, ss1967317136, ss2026578360, ss2154867121, ss2344080138, ss2627761578, ss2632813665, ss2699143507, ss2710731415, ss2897317304, ss3007741106, ss3021318078, ss3349496949, ss3625597911, ss3626621135, ss3630832255, ss3632979527, ss3633678414, ss3634445862, ss3635370208, ss3636130133, ss3637121030, ss3637896730, ss3640153201, ss3641012892, ss3641307294, ss3644558193, ss3651680780, ss3675142337, ss3737999715, ss3744082332, ss3744746764, ss3749052973, ss3772246798, ss3786895165, ss3792045090, ss3796927179, ss3832526520, ss3839812495, ss3875831789, ss3924076046, ss3984647820, ss3985524540, ss4017528599, ss5201072883 NC_000011.9:23214879:A:G NC_000011.10:23193333:A:G (self)
570261, 25758781, 834345, 58884268, 93800087, 5054679372, ss2180909740, ss3027086675, ss3139324959, ss3649556250, ss3691387362, ss3725225429, ss3771612876, ss3814401252, ss3845289502, ss3969380780, ss4878254431 NC_000011.10:23193333:A:G NC_000011.10:23193333:A:G (self)
ss15603454, ss18468174, ss18693497 NT_009237.16:21978819:A:G NC_000011.10:23193333:A:G (self)
ss23679664, ss39958845, ss66903706, ss67026009, ss68091195, ss70501186, ss71027134, ss75766899, ss85010657, ss97370689, ss106727949, ss132361237, ss137775761, ss152841137, ss156043010, ss159146200, ss159927122, ss170611600 NT_009237.18:23154879:A:G NC_000011.10:23193333:A:G (self)
5054679372 NC_000011.10:23193333:A:T NC_000011.10:23193333:A:T
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 rs10833965

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.post596+ae089ad