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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.

rs673709

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr18:42958712 (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>C
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.184072 (48722/264690, TOPMED)
G=0.266851 (55670/208618, ALFA)
G=0.193390 (27065/139950, GnomAD) (+ 19 more)
G=0.11866 (3353/28258, 14KJPN)
G=0.11718 (1964/16760, 8.3KJPN)
G=0.1657 (1061/6404, 1000G_30x)
G=0.1671 (837/5008, 1000G)
G=0.2482 (1112/4480, Estonian)
G=0.2735 (1054/3854, ALSPAC)
G=0.2621 (972/3708, TWINSUK)
G=0.1324 (388/2930, KOREAN)
G=0.1862 (388/2084, HGDP_Stanford)
G=0.1299 (245/1886, HapMap)
G=0.1365 (250/1832, Korea1K)
G=0.3037 (345/1136, Daghestan)
G=0.283 (282/998, GoNL)
G=0.217 (130/600, NorthernSweden)
G=0.119 (64/536, SGDP_PRJ)
G=0.338 (73/216, Qatari)
G=0.104 (22/212, Vietnamese)
G=0.16 (12/76, Ancient Sardinia)
G=0.19 (10/54, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
RIT2 : 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 208712 G=0.266904 A=0.733096, C=0.000000
European Sub 183030 G=0.280610 A=0.719390, C=0.000000
African Sub 8686 G=0.0488 A=0.9512, C=0.0000
African Others Sub 296 G=0.010 A=0.990, C=0.000
African American Sub 8390 G=0.0502 A=0.9498, C=0.0000
Asian Sub 570 G=0.100 A=0.900, C=0.000
East Asian Sub 490 G=0.098 A=0.902, C=0.000
Other Asian Sub 80 G=0.11 A=0.89, C=0.00
Latin American 1 Sub 690 G=0.177 A=0.823, C=0.000
Latin American 2 Sub 5574 G=0.1677 A=0.8323, C=0.0000
South Asian Sub 5022 G=0.3110 A=0.6890, C=0.0000
Other Sub 5140 G=0.2424 A=0.7576, C=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 G=0.184072 A=0.815928
Allele Frequency Aggregator Total Global 208618 G=0.266851 A=0.733149, C=0.000000
Allele Frequency Aggregator European Sub 182954 G=0.280568 A=0.719432, C=0.000000
Allele Frequency Aggregator African Sub 8686 G=0.0488 A=0.9512, C=0.0000
Allele Frequency Aggregator Latin American 2 Sub 5574 G=0.1677 A=0.8323, C=0.0000
Allele Frequency Aggregator Other Sub 5122 G=0.2419 A=0.7581, C=0.0000
Allele Frequency Aggregator South Asian Sub 5022 G=0.3110 A=0.6890, C=0.0000
Allele Frequency Aggregator Latin American 1 Sub 690 G=0.177 A=0.823, C=0.000
Allele Frequency Aggregator Asian Sub 570 G=0.100 A=0.900, C=0.000
gnomAD - Genomes Global Study-wide 139950 G=0.193390 A=0.806610
gnomAD - Genomes European Sub 75804 G=0.27165 A=0.72835
gnomAD - Genomes African Sub 41936 G=0.05277 A=0.94723
gnomAD - Genomes American Sub 13622 G=0.18771 A=0.81229
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.3051 A=0.6949
gnomAD - Genomes East Asian Sub 3118 G=0.0818 A=0.9182
gnomAD - Genomes Other Sub 2150 G=0.2023 A=0.7977
14KJPN JAPANESE Study-wide 28258 G=0.11866 A=0.88134
8.3KJPN JAPANESE Study-wide 16760 G=0.11718 A=0.88282
1000Genomes_30x Global Study-wide 6404 G=0.1657 A=0.8343
1000Genomes_30x African Sub 1786 G=0.0118 A=0.9882
1000Genomes_30x Europe Sub 1266 G=0.2709 A=0.7291
1000Genomes_30x South Asian Sub 1202 G=0.3037 A=0.6963
1000Genomes_30x East Asian Sub 1170 G=0.1085 A=0.8915
1000Genomes_30x American Sub 980 G=0.209 A=0.791
1000Genomes Global Study-wide 5008 G=0.1671 A=0.8329
1000Genomes African Sub 1322 G=0.0106 A=0.9894
1000Genomes East Asian Sub 1008 G=0.1071 A=0.8929
1000Genomes Europe Sub 1006 G=0.2694 A=0.7306
1000Genomes South Asian Sub 978 G=0.307 A=0.693
1000Genomes American Sub 694 G=0.207 A=0.793
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.2482 A=0.7518
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.2735 A=0.7265
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.2621 A=0.7379
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.1324 A=0.8676
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.1862 A=0.8138
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.094 A=0.906
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.302 A=0.698
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.271 A=0.729
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.328 A=0.672
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.000 A=1.000
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.088 A=0.912
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.00 A=1.00
HapMap Global Study-wide 1886 G=0.1299 A=0.8701
HapMap American Sub 768 G=0.203 A=0.797
HapMap African Sub 688 G=0.013 A=0.987
HapMap Asian Sub 254 G=0.094 A=0.906
HapMap Europe Sub 176 G=0.318 A=0.682
Korean Genome Project KOREAN Study-wide 1832 G=0.1365 A=0.8635
Genome-wide autozygosity in Daghestan Global Study-wide 1136 G=0.3037 A=0.6963
Genome-wide autozygosity in Daghestan Daghestan Sub 628 G=0.315 A=0.685
Genome-wide autozygosity in Daghestan Near_East Sub 144 G=0.243 A=0.757
Genome-wide autozygosity in Daghestan Central Asia Sub 122 G=0.279 A=0.721
Genome-wide autozygosity in Daghestan Europe Sub 108 G=0.241 A=0.759
Genome-wide autozygosity in Daghestan South Asian Sub 98 G=0.36 A=0.64
Genome-wide autozygosity in Daghestan Caucasus Sub 36 G=0.47 A=0.53
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.283 A=0.717
Northern Sweden ACPOP Study-wide 600 G=0.217 A=0.783
SGDP_PRJ Global Study-wide 536 G=0.119 A=0.881
Qatari Global Study-wide 216 G=0.338 A=0.662
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.104 A=0.896
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 76 G=0.16 A=0.84
Siberian Global Study-wide 54 G=0.19 A=0.81
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 18 NC_000018.10:g.42958712G>A
GRCh38.p14 chr 18 NC_000018.10:g.42958712G>C
GRCh37.p13 chr 18 NC_000018.9:g.40538677G>A
GRCh37.p13 chr 18 NC_000018.9:g.40538677G>C
Gene: RIT2, Ras like without CAAX 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
RIT2 transcript variant 2 NM_001272077.2:c.234+1536…

NM_001272077.2:c.234+15362C>T

 		N/A Intron Variant
RIT2 transcript variant 1 NM_002930.4:c.234+15362C>T 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 G= A C
GRCh38.p14 chr 18 NC_000018.10:g.42958712= NC_000018.10:g.42958712G>A NC_000018.10:g.42958712G>C
GRCh37.p13 chr 18 NC_000018.9:g.40538677= NC_000018.9:g.40538677G>A NC_000018.9:g.40538677G>C
RIT2 transcript variant 2 NM_001272077.1:c.234+15362= NM_001272077.1:c.234+15362C>T NM_001272077.1:c.234+15362C>G
RIT2 transcript variant 2 NM_001272077.2:c.234+15362= NM_001272077.2:c.234+15362C>T NM_001272077.2:c.234+15362C>G
RIT2 transcript variant 1 NM_002930.3:c.234+15362= NM_002930.3:c.234+15362C>T NM_002930.3:c.234+15362C>G
RIT2 transcript variant 1 NM_002930.4:c.234+15362= NM_002930.4:c.234+15362C>T NM_002930.4:c.234+15362C>G
RIT2 transcript variant X1 XM_005258327.1:c.177+15362= XM_005258327.1:c.177+15362C>T XM_005258327.1:c.177+15362C>G
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#.

125 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss847145 Aug 11, 2000 (83)
2 SC_JCM ss2655237 Nov 08, 2000 (89)
3 WI_SSAHASNP ss14411061 Dec 05, 2003 (119)
4 CSHL-HAPMAP ss19386948 Feb 27, 2004 (120)
5 SSAHASNP ss21452209 Apr 05, 2004 (123)
6 PERLEGEN ss24484553 Sep 20, 2004 (123)
7 ABI ss44140241 Mar 14, 2006 (126)
8 ILLUMINA ss66656132 Nov 30, 2006 (127)
9 ILLUMINA ss67491937 Nov 30, 2006 (127)
10 ILLUMINA ss67851279 Nov 30, 2006 (127)
11 PERLEGEN ss69212675 May 17, 2007 (127)
12 ILLUMINA ss70883222 May 26, 2008 (130)
13 ILLUMINA ss71474413 May 17, 2007 (127)
14 ILLUMINA ss75543950 Dec 06, 2007 (129)
15 ILLUMINA ss79231809 Dec 15, 2007 (130)
16 KRIBB_YJKIM ss83514358 Dec 15, 2007 (130)
17 BCMHGSC_JDW ss90774662 Mar 24, 2008 (129)
18 HUMANGENOME_JCVI ss96337893 Feb 06, 2009 (130)
19 BGI ss106542161 Feb 06, 2009 (130)
20 1000GENOMES ss110441199 Jan 24, 2009 (130)
21 1000GENOMES ss114321476 Jan 25, 2009 (130)
22 ILLUMINA-UK ss117855536 Feb 14, 2009 (130)
23 ILLUMINA ss122606188 Dec 01, 2009 (131)
24 ENSEMBL ss132679617 Dec 01, 2009 (131)
25 ENSEMBL ss137354382 Dec 01, 2009 (131)
26 ILLUMINA ss154379043 Dec 01, 2009 (131)
27 GMI ss155098007 Dec 01, 2009 (131)
28 ILLUMINA ss159554900 Dec 01, 2009 (131)
29 ILLUMINA ss160804152 Dec 01, 2009 (131)
30 COMPLETE_GENOMICS ss168128543 Jul 04, 2010 (132)
31 COMPLETE_GENOMICS ss169655643 Jul 04, 2010 (132)
32 ILLUMINA ss172182439 Jul 04, 2010 (132)
33 ILLUMINA ss174091490 Jul 04, 2010 (132)
34 BUSHMAN ss203207706 Jul 04, 2010 (132)
35 BCM-HGSC-SUB ss208053789 Jul 04, 2010 (132)
36 1000GENOMES ss227839845 Jul 14, 2010 (132)
37 1000GENOMES ss237450963 Jul 15, 2010 (132)
38 1000GENOMES ss243703544 Jul 15, 2010 (132)
39 BL ss255623923 May 09, 2011 (134)
40 GMI ss282976369 May 04, 2012 (137)
41 GMI ss287276612 Apr 25, 2013 (138)
42 PJP ss292163262 May 09, 2011 (134)
43 ILLUMINA ss481337034 May 04, 2012 (137)
44 ILLUMINA ss481362499 May 04, 2012 (137)
45 ILLUMINA ss482342628 Sep 08, 2015 (146)
46 ILLUMINA ss485463638 May 04, 2012 (137)
47 TISHKOFF ss565618725 Apr 25, 2013 (138)
48 SSMP ss661448743 Apr 25, 2013 (138)
49 ILLUMINA ss783177303 Sep 08, 2015 (146)
50 ILLUMINA ss825562327 Apr 01, 2015 (144)
51 ILLUMINA ss832436919 Sep 08, 2015 (146)
52 ILLUMINA ss833066066 Jul 13, 2019 (153)
53 EVA-GONL ss993690117 Aug 21, 2014 (142)
54 JMKIDD_LAB ss1081472681 Aug 21, 2014 (142)
55 1000GENOMES ss1360885805 Aug 21, 2014 (142)
56 HAMMER_LAB ss1397744579 Sep 08, 2015 (146)
57 DDI ss1428205225 Apr 01, 2015 (144)
58 EVA_UK10K_ALSPAC ss1636795699 Apr 01, 2015 (144)
59 EVA_UK10K_TWINSUK ss1679789732 Apr 01, 2015 (144)
60 EVA_DECODE ss1697746631 Apr 01, 2015 (144)
61 EVA_SVP ss1713623099 Apr 01, 2015 (144)
62 ILLUMINA ss1752255815 Sep 08, 2015 (146)
63 HAMMER_LAB ss1809035489 Sep 08, 2015 (146)
64 WEILL_CORNELL_DGM ss1937158742 Feb 12, 2016 (147)
65 GENOMED ss1968515056 Jul 19, 2016 (147)
66 JJLAB ss2029348566 Sep 14, 2016 (149)
67 USC_VALOUEV ss2157852996 Dec 20, 2016 (150)
68 HUMAN_LONGEVITY ss2221282198 Dec 20, 2016 (150)
69 SYSTEMSBIOZJU ss2629172383 Nov 08, 2017 (151)
70 ILLUMINA ss2633468403 Nov 08, 2017 (151)
71 GRF ss2702439015 Nov 08, 2017 (151)
72 ILLUMINA ss2710867074 Nov 08, 2017 (151)
73 GNOMAD ss2956296587 Nov 08, 2017 (151)
74 AFFY ss2985116980 Nov 08, 2017 (151)
75 AFFY ss2985753111 Nov 08, 2017 (151)
76 SWEGEN ss3016469852 Nov 08, 2017 (151)
77 BIOINF_KMB_FNS_UNIBA ss3028501835 Nov 08, 2017 (151)
78 CSHL ss3352006476 Nov 08, 2017 (151)
79 ILLUMINA ss3633161260 Oct 12, 2018 (152)
80 ILLUMINA ss3633869995 Oct 12, 2018 (152)
81 ILLUMINA ss3634704429 Oct 12, 2018 (152)
82 ILLUMINA ss3635557303 Oct 12, 2018 (152)
83 ILLUMINA ss3636393678 Oct 12, 2018 (152)
84 ILLUMINA ss3637308911 Oct 12, 2018 (152)
85 ILLUMINA ss3638194089 Oct 12, 2018 (152)
86 ILLUMINA ss3639105057 Oct 12, 2018 (152)
87 ILLUMINA ss3639560954 Oct 12, 2018 (152)
88 ILLUMINA ss3640411737 Oct 12, 2018 (152)
89 ILLUMINA ss3643170045 Oct 12, 2018 (152)
90 URBANLAB ss3650782853 Oct 12, 2018 (152)
91 ILLUMINA ss3653889168 Oct 12, 2018 (152)
92 EGCUT_WGS ss3683308501 Jul 13, 2019 (153)
93 EVA_DECODE ss3701589773 Jul 13, 2019 (153)
94 ACPOP ss3742512601 Jul 13, 2019 (153)
95 ILLUMINA ss3745004577 Jul 13, 2019 (153)
96 EVA ss3755343956 Jul 13, 2019 (153)
97 ILLUMINA ss3772502088 Jul 13, 2019 (153)
98 PACBIO ss3788360827 Jul 13, 2019 (153)
99 PACBIO ss3793293298 Jul 13, 2019 (153)
100 PACBIO ss3798179643 Jul 13, 2019 (153)
101 KHV_HUMAN_GENOMES ss3820609099 Jul 13, 2019 (153)
102 EVA ss3835151350 Apr 27, 2020 (154)
103 EVA ss3841192822 Apr 27, 2020 (154)
104 EVA ss3846694823 Apr 27, 2020 (154)
105 HGDP ss3847582077 Apr 27, 2020 (154)
106 SGDP_PRJ ss3886947419 Apr 27, 2020 (154)
107 KRGDB ss3936809470 Apr 27, 2020 (154)
108 KOGIC ss3980083586 Apr 27, 2020 (154)
109 EVA ss3985823573 Apr 26, 2021 (155)
110 TOPMED ss5055472040 Apr 26, 2021 (155)
111 TOMMO_GENOMICS ss5225014999 Apr 26, 2021 (155)
112 1000G_HIGH_COVERAGE ss5305173677 Oct 16, 2022 (156)
113 EVA ss5315930231 Oct 16, 2022 (156)
114 EVA ss5431199376 Oct 16, 2022 (156)
115 HUGCELL_USP ss5497956662 Oct 16, 2022 (156)
116 1000G_HIGH_COVERAGE ss5609953659 Oct 16, 2022 (156)
117 SANFORD_IMAGENETICS ss5661227458 Oct 16, 2022 (156)
118 TOMMO_GENOMICS ss5782761756 Oct 16, 2022 (156)
119 EVA ss5799992331 Oct 16, 2022 (156)
120 YY_MCH ss5817066266 Oct 16, 2022 (156)
121 EVA ss5827495742 Oct 16, 2022 (156)
122 EVA ss5852038090 Oct 16, 2022 (156)
123 EVA ss5873942241 Oct 16, 2022 (156)
124 EVA ss5952637060 Oct 16, 2022 (156)
125 EVA ss5981005296 Oct 16, 2022 (156)
126 1000Genomes NC_000018.9 - 40538677 Oct 12, 2018 (152)
127 1000Genomes_30x NC_000018.10 - 42958712 Oct 16, 2022 (156)
128 The Avon Longitudinal Study of Parents and Children NC_000018.9 - 40538677 Oct 12, 2018 (152)
129 Genome-wide autozygosity in Daghestan NC_000018.8 - 38792675 Apr 27, 2020 (154)
130 Genetic variation in the Estonian population NC_000018.9 - 40538677 Oct 12, 2018 (152)
131 gnomAD - Genomes NC_000018.10 - 42958712 Apr 26, 2021 (155)
132 Genome of the Netherlands Release 5 NC_000018.9 - 40538677 Apr 27, 2020 (154)
133 HGDP-CEPH-db Supplement 1 NC_000018.8 - 38792675 Apr 27, 2020 (154)
134 HapMap NC_000018.10 - 42958712 Apr 27, 2020 (154)
135 KOREAN population from KRGDB NC_000018.9 - 40538677 Apr 27, 2020 (154)
136 Korean Genome Project NC_000018.10 - 42958712 Apr 27, 2020 (154)
137 Northern Sweden NC_000018.9 - 40538677 Jul 13, 2019 (153)
138 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000018.9 - 40538677 Apr 26, 2021 (155)
139 Qatari NC_000018.9 - 40538677 Apr 27, 2020 (154)
140 SGDP_PRJ NC_000018.9 - 40538677 Apr 27, 2020 (154)
141 Siberian NC_000018.9 - 40538677 Apr 27, 2020 (154)
142 8.3KJPN NC_000018.9 - 40538677 Apr 26, 2021 (155)
143 14KJPN NC_000018.10 - 42958712 Oct 16, 2022 (156)
144 TopMed NC_000018.10 - 42958712 Apr 26, 2021 (155)
145 UK 10K study - Twins NC_000018.9 - 40538677 Oct 12, 2018 (152)
146 A Vietnamese Genetic Variation Database NC_000018.9 - 40538677 Jul 13, 2019 (153)
147 ALFA NC_000018.10 - 42958712 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)
rs12957419 Sep 24, 2004 (123)
rs17643256 Oct 08, 2004 (123)
rs56622388 May 26, 2008 (130)
rs60410196 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
214281, 259969, ss90774662, ss110441199, ss114321476, ss117855536, ss168128543, ss169655643, ss203207706, ss208053789, ss255623923, ss282976369, ss287276612, ss292163262, ss481337034, ss825562327, ss1397744579, ss1697746631, ss1713623099, ss3639105057, ss3639560954, ss3643170045, ss3847582077 NC_000018.8:38792674:G:A NC_000018.10:42958711:G:A (self)
74210398, 41111960, 29046749, 18318482, 43986864, 15797466, 1049500, 19200664, 38964399, 10369350, 82984306, 41111960, 9084051, ss227839845, ss237450963, ss243703544, ss481362499, ss482342628, ss485463638, ss565618725, ss661448743, ss783177303, ss832436919, ss833066066, ss993690117, ss1081472681, ss1360885805, ss1428205225, ss1636795699, ss1679789732, ss1752255815, ss1809035489, ss1937158742, ss1968515056, ss2029348566, ss2157852996, ss2629172383, ss2633468403, ss2702439015, ss2710867074, ss2956296587, ss2985116980, ss2985753111, ss3016469852, ss3352006476, ss3633161260, ss3633869995, ss3634704429, ss3635557303, ss3636393678, ss3637308911, ss3638194089, ss3640411737, ss3653889168, ss3683308501, ss3742512601, ss3745004577, ss3755343956, ss3772502088, ss3788360827, ss3793293298, ss3798179643, ss3835151350, ss3841192822, ss3886947419, ss3936809470, ss3985823573, ss5225014999, ss5315930231, ss5431199376, ss5661227458, ss5799992331, ss5827495742, ss5952637060, ss5981005296 NC_000018.9:40538676:G:A NC_000018.10:42958711:G:A (self)
97479594, 523538152, 1594583, 36461587, 116598860, 271017703, 7849607507, ss2221282198, ss3028501835, ss3650782853, ss3701589773, ss3820609099, ss3846694823, ss3980083586, ss5055472040, ss5305173677, ss5497956662, ss5609953659, ss5782761756, ss5817066266, ss5852038090, ss5873942241 NC_000018.10:42958711:G:A NC_000018.10:42958711:G:A (self)
ss14411061, ss19386948, ss21452209 NT_010966.13:22027778:G:A NC_000018.10:42958711:G:A (self)
ss847145, ss2655237, ss24484553, ss44140241, ss66656132, ss67491937, ss67851279, ss69212675, ss70883222, ss71474413, ss75543950, ss79231809, ss83514358, ss96337893, ss106542161, ss122606188, ss132679617, ss137354382, ss154379043, ss155098007, ss159554900, ss160804152, ss172182439, ss174091490 NT_010966.14:22027778:G:A NC_000018.10:42958711:G:A (self)
7849607507 NC_000018.10:42958711:G:C NC_000018.10:42958711:G:C (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 rs673709

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