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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs7192196

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr16:78326766 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.483184 (127894/264690, TOPMED)
A=0.386608 (83355/215606, ALFA)
A=0.479279 (66986/139764, GnomAD) (+ 20 more)
G=0.44224 (34765/78612, PAGE_STUDY)
G=0.41730 (11792/28258, 14KJPN)
G=0.41874 (7018/16760, 8.3KJPN)
G=0.4967 (3181/6404, 1000G_30x)
G=0.4970 (2489/5008, 1000G)
A=0.4092 (1833/4480, Estonian)
A=0.3770 (1453/3854, ALSPAC)
A=0.3792 (1406/3708, TWINSUK)
G=0.4136 (1211/2928, KOREAN)
A=0.4784 (997/2084, HGDP_Stanford)
G=0.4868 (919/1888, HapMap)
A=0.381 (380/998, GoNL)
A=0.427 (256/600, NorthernSweden)
G=0.291 (117/402, SGDP_PRJ)
A=0.329 (71/216, Qatari)
G=0.380 (82/216, Vietnamese)
G=0.32 (14/44, Siberian)
G=0.50 (20/40, GENOME_DK)
A=0.50 (20/40, GENOME_DK)
A=0.38 (12/32, Ancient Sardinia)
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 215606 G=0.613392 A=0.386608
European Sub 187554 G=0.626657 A=0.373343
African Sub 7504 G=0.3250 A=0.6750
African Others Sub 264 G=0.220 A=0.780
African American Sub 7240 G=0.3289 A=0.6711
Asian Sub 780 G=0.391 A=0.609
East Asian Sub 634 G=0.397 A=0.603
Other Asian Sub 146 G=0.363 A=0.637
Latin American 1 Sub 844 G=0.572 A=0.428
Latin American 2 Sub 6854 G=0.5871 A=0.4129
South Asian Sub 5024 G=0.6728 A=0.3272
Other Sub 7046 G=0.5802 A=0.4198


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=0.516816 A=0.483184
Allele Frequency Aggregator Total Global 215606 G=0.613392 A=0.386608
Allele Frequency Aggregator European Sub 187554 G=0.626657 A=0.373343
Allele Frequency Aggregator African Sub 7504 G=0.3250 A=0.6750
Allele Frequency Aggregator Other Sub 7046 G=0.5802 A=0.4198
Allele Frequency Aggregator Latin American 2 Sub 6854 G=0.5871 A=0.4129
Allele Frequency Aggregator South Asian Sub 5024 G=0.6728 A=0.3272
Allele Frequency Aggregator Latin American 1 Sub 844 G=0.572 A=0.428
Allele Frequency Aggregator Asian Sub 780 G=0.391 A=0.609
gnomAD - Genomes Global Study-wide 139764 G=0.520721 A=0.479279
gnomAD - Genomes European Sub 75726 G=0.61189 A=0.38811
gnomAD - Genomes African Sub 41864 G=0.33301 A=0.66699
gnomAD - Genomes American Sub 13600 G=0.57618 A=0.42382
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.6578 A=0.3422
gnomAD - Genomes East Asian Sub 3108 G=0.4160 A=0.5840
gnomAD - Genomes Other Sub 2146 G=0.5536 A=0.4464
The PAGE Study Global Study-wide 78612 G=0.44224 A=0.55776
The PAGE Study AfricanAmerican Sub 32464 G=0.34395 A=0.65605
The PAGE Study Mexican Sub 10796 G=0.58086 A=0.41914
The PAGE Study Asian Sub 8318 G=0.4108 A=0.5892
The PAGE Study PuertoRican Sub 7914 G=0.5288 A=0.4712
The PAGE Study NativeHawaiian Sub 4530 G=0.3830 A=0.6170
The PAGE Study Cuban Sub 4222 G=0.5867 A=0.4133
The PAGE Study Dominican Sub 3824 G=0.4799 A=0.5201
The PAGE Study CentralAmerican Sub 2450 G=0.5347 A=0.4653
The PAGE Study SouthAmerican Sub 1980 G=0.5621 A=0.4379
The PAGE Study NativeAmerican Sub 1258 G=0.5644 A=0.4356
The PAGE Study SouthAsian Sub 856 G=0.638 A=0.362
14KJPN JAPANESE Study-wide 28258 G=0.41730 A=0.58270
8.3KJPN JAPANESE Study-wide 16760 G=0.41874 A=0.58126
1000Genomes_30x Global Study-wide 6404 G=0.4967 A=0.5033
1000Genomes_30x African Sub 1786 G=0.3085 A=0.6915
1000Genomes_30x Europe Sub 1266 G=0.6161 A=0.3839
1000Genomes_30x South Asian Sub 1202 G=0.6539 A=0.3461
1000Genomes_30x East Asian Sub 1170 G=0.4265 A=0.5735
1000Genomes_30x American Sub 980 G=0.577 A=0.423
1000Genomes Global Study-wide 5008 G=0.4970 A=0.5030
1000Genomes African Sub 1322 G=0.3011 A=0.6989
1000Genomes East Asian Sub 1008 G=0.4296 A=0.5704
1000Genomes Europe Sub 1006 G=0.6103 A=0.3897
1000Genomes South Asian Sub 978 G=0.664 A=0.336
1000Genomes American Sub 694 G=0.569 A=0.431
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.5908 A=0.4092
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.6230 A=0.3770
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.6208 A=0.3792
KOREAN population from KRGDB KOREAN Study-wide 2928 G=0.4136 A=0.5864
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.5216 A=0.4784
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.379 A=0.621
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.618 A=0.382
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.643 A=0.357
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.631 A=0.369
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.293 A=0.707
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.486 A=0.514
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.69 A=0.31
HapMap Global Study-wide 1888 G=0.4868 A=0.5132
HapMap American Sub 770 G=0.538 A=0.462
HapMap African Sub 690 G=0.396 A=0.604
HapMap Asian Sub 252 G=0.468 A=0.532
HapMap Europe Sub 176 G=0.648 A=0.352
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.619 A=0.381
Northern Sweden ACPOP Study-wide 600 G=0.573 A=0.427
SGDP_PRJ Global Study-wide 402 G=0.291 A=0.709
Qatari Global Study-wide 216 G=0.671 A=0.329
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.380 A=0.620
Siberian Global Study-wide 44 G=0.32 A=0.68
The Danish reference pan genome Danish Study-wide 40 G=0.50 A=0.50
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 32 G=0.62 A=0.38
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.78326766G>A
GRCh37.p13 chr 16 NC_000016.9:g.78360663G>A
WWOX RefSeqGene NG_011698.1:g.232113G>A
Gene: WWOX, WW domain containing oxidoreductase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
WWOX transcript variant 4 NM_001291997.2:c.178-6009…

NM_001291997.2:c.178-60094G>A

 		N/A Intron Variant
WWOX transcript variant 1 NM_016373.4:c.517-60094G>A 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 G= A
GRCh38.p14 chr 16 NC_000016.10:g.78326766= NC_000016.10:g.78326766G>A
GRCh37.p13 chr 16 NC_000016.9:g.78360663= NC_000016.9:g.78360663G>A
WWOX RefSeqGene NG_011698.1:g.232113= NG_011698.1:g.232113G>A
WWOX transcript variant 4 NM_001291997.2:c.178-60094= NM_001291997.2:c.178-60094G>A
WWOX transcript variant 1 NM_016373.2:c.517-60094= NM_016373.2:c.517-60094G>A
WWOX transcript variant 1 NM_016373.4:c.517-60094= NM_016373.4:c.517-60094G>A
WWOX transcript variant X1 XM_005255980.1:c.409+211612= XM_005255980.1:c.409+211612G>A
WWOX transcript variant X2 XM_005255981.1:c.178-60094= XM_005255981.1:c.178-60094G>A
WWOX transcript variant X3 XM_005255982.1:c.516+162477= XM_005255982.1:c.516+162477G>A
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#.

120 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10819067 Jul 11, 2003 (116)
2 CSHL-HAPMAP ss16703414 Feb 27, 2004 (120)
3 ABI ss43948372 Mar 15, 2006 (126)
4 ILLUMINA ss66722822 Dec 01, 2006 (127)
5 ILLUMINA ss67553771 Dec 01, 2006 (127)
6 ILLUMINA ss67929256 Dec 01, 2006 (127)
7 ILLUMINA ss70915022 May 25, 2008 (130)
8 ILLUMINA ss71513533 May 18, 2007 (127)
9 ILLUMINA ss75622165 Dec 05, 2007 (129)
10 ILLUMINA ss79249377 Dec 15, 2007 (130)
11 KRIBB_YJKIM ss84634344 Dec 15, 2007 (130)
12 BCMHGSC_JDW ss90455453 Mar 24, 2008 (129)
13 BGI ss103311636 Dec 01, 2009 (131)
14 1000GENOMES ss109464391 Jan 24, 2009 (130)
15 1000GENOMES ss115349133 Jan 25, 2009 (130)
16 ILLUMINA-UK ss118318862 Feb 14, 2009 (130)
17 ILLUMINA ss122711117 Dec 01, 2009 (131)
18 ENSEMBL ss136821097 Dec 01, 2009 (131)
19 ILLUMINA ss154411354 Dec 01, 2009 (131)
20 GMI ss157577812 Dec 01, 2009 (131)
21 ILLUMINA ss159586451 Dec 01, 2009 (131)
22 ILLUMINA ss160858298 Dec 01, 2009 (131)
23 ENSEMBL ss161805261 Dec 01, 2009 (131)
24 COMPLETE_GENOMICS ss168509347 Jul 04, 2010 (132)
25 COMPLETE_GENOMICS ss170268724 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss171519188 Jul 04, 2010 (132)
27 ILLUMINA ss172259131 Jul 04, 2010 (132)
28 ILLUMINA ss174282785 Jul 04, 2010 (132)
29 BUSHMAN ss201925311 Jul 04, 2010 (132)
30 BCM-HGSC-SUB ss207530044 Jul 04, 2010 (132)
31 1000GENOMES ss227340659 Jul 14, 2010 (132)
32 1000GENOMES ss237096424 Jul 15, 2010 (132)
33 1000GENOMES ss243422460 Jul 15, 2010 (132)
34 GMI ss282606169 May 04, 2012 (137)
35 GMI ss287107823 Apr 25, 2013 (138)
36 PJP ss291879032 May 09, 2011 (134)
37 ILLUMINA ss481499746 May 04, 2012 (137)
38 ILLUMINA ss481528304 May 04, 2012 (137)
39 ILLUMINA ss482504378 Sep 08, 2015 (146)
40 ILLUMINA ss485545010 May 04, 2012 (137)
41 ILLUMINA ss537448024 Sep 08, 2015 (146)
42 TISHKOFF ss565019714 Apr 25, 2013 (138)
43 SSMP ss660799794 Apr 25, 2013 (138)
44 ILLUMINA ss778596084 Sep 08, 2015 (146)
45 ILLUMINA ss783218052 Sep 08, 2015 (146)
46 ILLUMINA ss784172597 Sep 08, 2015 (146)
47 ILLUMINA ss825579895 Apr 01, 2015 (144)
48 ILLUMINA ss832478251 Sep 08, 2015 (146)
49 ILLUMINA ss833097488 Jul 13, 2019 (153)
50 ILLUMINA ss834053327 Sep 08, 2015 (146)
51 EVA-GONL ss992692257 Aug 21, 2014 (142)
52 JMKIDD_LAB ss1080766449 Aug 21, 2014 (142)
53 1000GENOMES ss1357025608 Aug 21, 2014 (142)
54 DDI ss1427902570 Apr 01, 2015 (144)
55 EVA_GENOME_DK ss1577993246 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1634837981 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1677832014 Apr 01, 2015 (144)
58 EVA_SVP ss1713552898 Apr 01, 2015 (144)
59 ILLUMINA ss1752205111 Sep 08, 2015 (146)
60 HAMMER_LAB ss1808598252 Sep 08, 2015 (146)
61 WEILL_CORNELL_DGM ss1936122491 Feb 12, 2016 (147)
62 ILLUMINA ss1959697843 Feb 12, 2016 (147)
63 GENOMED ss1968303859 Jul 19, 2016 (147)
64 JJLAB ss2028848056 Sep 14, 2016 (149)
65 USC_VALOUEV ss2157289574 Dec 20, 2016 (150)
66 HUMAN_LONGEVITY ss2213769392 Dec 20, 2016 (150)
67 SYSTEMSBIOZJU ss2628916182 Nov 08, 2017 (151)
68 ILLUMINA ss2633342072 Nov 08, 2017 (151)
69 GRF ss2701821858 Nov 08, 2017 (151)
70 ILLUMINA ss2710838007 Nov 08, 2017 (151)
71 GNOMAD ss2945277078 Nov 08, 2017 (151)
72 SWEGEN ss3014834251 Nov 08, 2017 (151)
73 ILLUMINA ss3021726838 Nov 08, 2017 (151)
74 BIOINF_KMB_FNS_UNIBA ss3028241014 Nov 08, 2017 (151)
75 CSHL ss3351540061 Nov 08, 2017 (151)
76 ILLUMINA ss3627568115 Oct 12, 2018 (152)
77 ILLUMINA ss3631326887 Oct 12, 2018 (152)
78 ILLUMINA ss3633126917 Oct 12, 2018 (152)
79 ILLUMINA ss3633833334 Oct 12, 2018 (152)
80 ILLUMINA ss3634651340 Oct 12, 2018 (152)
81 ILLUMINA ss3635521500 Oct 12, 2018 (152)
82 ILLUMINA ss3636342584 Oct 12, 2018 (152)
83 ILLUMINA ss3637272962 Oct 12, 2018 (152)
84 ILLUMINA ss3638136158 Oct 12, 2018 (152)
85 ILLUMINA ss3639078869 Oct 12, 2018 (152)
86 ILLUMINA ss3639545942 Oct 12, 2018 (152)
87 ILLUMINA ss3640358660 Oct 12, 2018 (152)
88 ILLUMINA ss3643116523 Oct 12, 2018 (152)
89 ILLUMINA ss3652138233 Oct 12, 2018 (152)
90 EGCUT_WGS ss3681811813 Jul 13, 2019 (153)
91 EVA_DECODE ss3699648774 Jul 13, 2019 (153)
92 ILLUMINA ss3725578701 Jul 13, 2019 (153)
93 ACPOP ss3741677002 Jul 13, 2019 (153)
94 ILLUMINA ss3744951761 Jul 13, 2019 (153)
95 EVA ss3754171097 Jul 13, 2019 (153)
96 PAGE_CC ss3771892962 Jul 13, 2019 (153)
97 ILLUMINA ss3772449934 Jul 13, 2019 (153)
98 KHV_HUMAN_GENOMES ss3819451491 Jul 13, 2019 (153)
99 EVA ss3834664918 Apr 27, 2020 (154)
100 EVA ss3840937943 Apr 27, 2020 (154)
101 EVA ss3846430808 Apr 27, 2020 (154)
102 HGDP ss3847551052 Apr 27, 2020 (154)
103 SGDP_PRJ ss3884849895 Apr 27, 2020 (154)
104 KRGDB ss3934392438 Apr 27, 2020 (154)
105 EVA ss3985767692 Apr 27, 2021 (155)
106 EVA ss4017745797 Apr 27, 2021 (155)
107 TOPMED ss5022326057 Apr 27, 2021 (155)
108 TOMMO_GENOMICS ss5220486405 Apr 27, 2021 (155)
109 1000G_HIGH_COVERAGE ss5301646701 Oct 17, 2022 (156)
110 EVA ss5315851983 Oct 17, 2022 (156)
111 HUGCELL_USP ss5494920272 Oct 17, 2022 (156)
112 1000G_HIGH_COVERAGE ss5604655419 Oct 17, 2022 (156)
113 SANFORD_IMAGENETICS ss5659282744 Oct 17, 2022 (156)
114 TOMMO_GENOMICS ss5775764214 Oct 17, 2022 (156)
115 EVA ss5799963005 Oct 17, 2022 (156)
116 YY_MCH ss5816138025 Oct 17, 2022 (156)
117 EVA ss5846676611 Oct 17, 2022 (156)
118 EVA ss5851644361 Oct 17, 2022 (156)
119 EVA ss5899871843 Oct 17, 2022 (156)
120 EVA ss5950687641 Oct 17, 2022 (156)
121 1000Genomes NC_000016.9 - 78360663 Oct 12, 2018 (152)
122 1000Genomes_30x NC_000016.10 - 78326766 Oct 17, 2022 (156)
123 The Avon Longitudinal Study of Parents and Children NC_000016.9 - 78360663 Oct 12, 2018 (152)
124 Genetic variation in the Estonian population NC_000016.9 - 78360663 Oct 12, 2018 (152)
125 The Danish reference pan genome NC_000016.9 - 78360663 Apr 27, 2020 (154)
126 gnomAD - Genomes NC_000016.10 - 78326766 Apr 27, 2021 (155)
127 Genome of the Netherlands Release 5 NC_000016.9 - 78360663 Apr 27, 2020 (154)
128 HGDP-CEPH-db Supplement 1 NC_000016.8 - 76918164 Apr 27, 2020 (154)
129 HapMap NC_000016.10 - 78326766 Apr 27, 2020 (154)
130 KOREAN population from KRGDB NC_000016.9 - 78360663 Apr 27, 2020 (154)
131 Northern Sweden NC_000016.9 - 78360663 Jul 13, 2019 (153)
132 The PAGE Study NC_000016.10 - 78326766 Jul 13, 2019 (153)
133 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000016.9 - 78360663 Apr 27, 2021 (155)
134 Qatari NC_000016.9 - 78360663 Apr 27, 2020 (154)
135 SGDP_PRJ NC_000016.9 - 78360663 Apr 27, 2020 (154)
136 Siberian NC_000016.9 - 78360663 Apr 27, 2020 (154)
137 8.3KJPN NC_000016.9 - 78360663 Apr 27, 2021 (155)
138 14KJPN NC_000016.10 - 78326766 Oct 17, 2022 (156)
139 TopMed NC_000016.10 - 78326766 Apr 27, 2021 (155)
140 UK 10K study - Twins NC_000016.9 - 78360663 Oct 12, 2018 (152)
141 A Vietnamese Genetic Variation Database NC_000016.9 - 78360663 Jul 13, 2019 (153)
142 ALFA NC_000016.10 - 78326766 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)
rs60215005 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
228944, ss90455453, ss109464391, ss115349133, ss118318862, ss168509347, ss170268724, ss171519188, ss201925311, ss207530044, ss282606169, ss287107823, ss291879032, ss481499746, ss825579895, ss1713552898, ss3639078869, ss3639545942, ss3643116523, ss3847551052 NC_000016.8:76918163:G:A NC_000016.10:78326765:G:A (self)
70214820, 38954154, 27550061, 4202408, 17365930, 41569832, 14961867, 993619, 18164413, 36866875, 9805928, 78455712, 38954154, 8634175, ss227340659, ss237096424, ss243422460, ss481528304, ss482504378, ss485545010, ss537448024, ss565019714, ss660799794, ss778596084, ss783218052, ss784172597, ss832478251, ss833097488, ss834053327, ss992692257, ss1080766449, ss1357025608, ss1427902570, ss1577993246, ss1634837981, ss1677832014, ss1752205111, ss1808598252, ss1936122491, ss1959697843, ss1968303859, ss2028848056, ss2157289574, ss2628916182, ss2633342072, ss2701821858, ss2710838007, ss2945277078, ss3014834251, ss3021726838, ss3351540061, ss3627568115, ss3631326887, ss3633126917, ss3633833334, ss3634651340, ss3635521500, ss3636342584, ss3637272962, ss3638136158, ss3640358660, ss3652138233, ss3681811813, ss3741677002, ss3744951761, ss3754171097, ss3772449934, ss3834664918, ss3840937943, ss3884849895, ss3934392438, ss3985767692, ss4017745797, ss5220486405, ss5315851983, ss5659282744, ss5799963005, ss5846676611, ss5950687641 NC_000016.9:78360662:G:A NC_000016.10:78326765:G:A (self)
92181354, 495377456, 1418197, 1114431, 109601318, 237871718, 888376897, ss2213769392, ss3028241014, ss3699648774, ss3725578701, ss3771892962, ss3819451491, ss3846430808, ss5022326057, ss5301646701, ss5494920272, ss5604655419, ss5775764214, ss5816138025, ss5851644361, ss5899871843 NC_000016.10:78326765:G:A NC_000016.10:78326765:G:A (self)
ss43948372, ss66722822, ss67553771, ss67929256, ss70915022, ss71513533, ss75622165, ss79249377, ss84634344, ss103311636, ss122711117, ss136821097, ss154411354, ss157577812, ss159586451, ss160858298, ss161805261, ss172259131, ss174282785 NT_010498.15:31974861:G:A NC_000016.10:78326765:G:A (self)
ss10819067 NT_024797.13:5072349:G:A NC_000016.10:78326765:G:A (self)
ss16703414 NT_024797.14:5072349:G:A NC_000016.10:78326765:G:A (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs7192196

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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
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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