Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs347518

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr19:43768036 (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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.065080 (17226/264690, TOPMED)
G=0.066863 (9378/140256, GnomAD)
G=0.07760 (3522/45386, ALFA) (+ 17 more)
G=0.04084 (1154/28258, 14KJPN)
G=0.04039 (677/16760, 8.3KJPN)
G=0.0703 (450/6404, 1000G_30x)
G=0.0713 (357/5008, 1000G)
G=0.0806 (361/4480, Estonian)
G=0.1020 (393/3854, ALSPAC)
G=0.0960 (356/3708, TWINSUK)
G=0.0560 (164/2930, KOREAN)
G=0.0677 (128/1892, HapMap)
G=0.0677 (124/1832, Korea1K)
G=0.091 (91/998, GoNL)
G=0.073 (44/600, NorthernSweden)
G=0.049 (27/556, SGDP_PRJ)
G=0.060 (13/216, Qatari)
G=0.065 (14/214, Vietnamese)
G=0.04 (2/56, Siberian)
G=0.07 (3/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
KCNN4 : 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 45386 G=0.07760 A=0.92240
European Sub 34118 G=0.08860 A=0.91140
African Sub 6252 G=0.0306 A=0.9694
African Others Sub 210 G=0.024 A=0.976
African American Sub 6042 G=0.0308 A=0.9692
Asian Sub 204 G=0.069 A=0.931
East Asian Sub 146 G=0.048 A=0.952
Other Asian Sub 58 G=0.12 A=0.88
Latin American 1 Sub 292 G=0.051 A=0.949
Latin American 2 Sub 2766 G=0.0474 A=0.9526
South Asian Sub 110 G=0.155 A=0.845
Other Sub 1644 G=0.0797 A=0.9203


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=0.065080 A=0.934920
gnomAD - Genomes Global Study-wide 140256 G=0.066863 A=0.933137
gnomAD - Genomes European Sub 75942 G=0.08954 A=0.91046
gnomAD - Genomes African Sub 42048 G=0.03089 A=0.96911
gnomAD - Genomes American Sub 13654 G=0.05508 A=0.94492
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.0773 A=0.9227
gnomAD - Genomes East Asian Sub 3134 G=0.0437 A=0.9563
gnomAD - Genomes Other Sub 2154 G=0.0617 A=0.9383
Allele Frequency Aggregator Total Global 45386 G=0.07760 A=0.92240
Allele Frequency Aggregator European Sub 34118 G=0.08860 A=0.91140
Allele Frequency Aggregator African Sub 6252 G=0.0306 A=0.9694
Allele Frequency Aggregator Latin American 2 Sub 2766 G=0.0474 A=0.9526
Allele Frequency Aggregator Other Sub 1644 G=0.0797 A=0.9203
Allele Frequency Aggregator Latin American 1 Sub 292 G=0.051 A=0.949
Allele Frequency Aggregator Asian Sub 204 G=0.069 A=0.931
Allele Frequency Aggregator South Asian Sub 110 G=0.155 A=0.845
14KJPN JAPANESE Study-wide 28258 G=0.04084 A=0.95916
8.3KJPN JAPANESE Study-wide 16760 G=0.04039 A=0.95961
1000Genomes_30x Global Study-wide 6404 G=0.0703 A=0.9297
1000Genomes_30x African Sub 1786 G=0.0168 A=0.9832
1000Genomes_30x Europe Sub 1266 G=0.0869 A=0.9131
1000Genomes_30x South Asian Sub 1202 G=0.1830 A=0.8170
1000Genomes_30x East Asian Sub 1170 G=0.0419 A=0.9581
1000Genomes_30x American Sub 980 G=0.042 A=0.958
1000Genomes Global Study-wide 5008 G=0.0713 A=0.9287
1000Genomes African Sub 1322 G=0.0136 A=0.9864
1000Genomes East Asian Sub 1008 G=0.0417 A=0.9583
1000Genomes Europe Sub 1006 G=0.0865 A=0.9135
1000Genomes South Asian Sub 978 G=0.184 A=0.816
1000Genomes American Sub 694 G=0.043 A=0.957
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.0806 A=0.9194
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.1020 A=0.8980
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.0960 A=0.9040
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.0560 A=0.9440, C=0.0000, T=0.0000
HapMap Global Study-wide 1892 G=0.0677 A=0.9323
HapMap American Sub 770 G=0.104 A=0.896
HapMap African Sub 692 G=0.027 A=0.973
HapMap Asian Sub 254 G=0.051 A=0.949
HapMap Europe Sub 176 G=0.091 A=0.909
Korean Genome Project KOREAN Study-wide 1832 G=0.0677 A=0.9323
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.091 A=0.909
Northern Sweden ACPOP Study-wide 600 G=0.073 A=0.927
SGDP_PRJ Global Study-wide 556 G=0.049 A=0.951
Qatari Global Study-wide 216 G=0.060 A=0.940
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.065 A=0.935
Siberian Global Study-wide 56 G=0.04 A=0.96
The Danish reference pan genome Danish Study-wide 40 G=0.07 A=0.93
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 19 NC_000019.10:g.43768036G>A
GRCh38.p14 chr 19 NC_000019.10:g.43768036G>C
GRCh38.p14 chr 19 NC_000019.10:g.43768036G>T
GRCh37.p13 chr 19 NC_000019.9:g.44272188G>A
GRCh37.p13 chr 19 NC_000019.9:g.44272188G>C
GRCh37.p13 chr 19 NC_000019.9:g.44272188G>T
KCNN4 RefSeqGene (LRG_1305) NG_052672.1:g.19104C>T
KCNN4 RefSeqGene (LRG_1305) NG_052672.1:g.19104C>G
KCNN4 RefSeqGene (LRG_1305) NG_052672.1:g.19104C>A
Gene: KCNN4, potassium calcium-activated channel subfamily N member 4 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
KCNN4 transcript NM_002250.3:c.1120-329C>T N/A Intron Variant
KCNN4 transcript variant X1 XM_005258882.3:c.1024-329…

XM_005258882.3:c.1024-329C>T

 		N/A Intron Variant
KCNN4 transcript variant X2 XM_005258883.3:c.931-329C…

XM_005258883.3:c.931-329C>T

 		N/A Intron Variant
KCNN4 transcript variant X5 XM_047438794.1:c.448-329C…

XM_047438794.1:c.448-329C>T

 		N/A Intron Variant
KCNN4 transcript variant X3 XM_047438793.1:c. N/A Genic Downstream Transcript Variant
KCNN4 transcript variant X4 XR_935823.2: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 C T
GRCh38.p14 chr 19 NC_000019.10:g.43768036= NC_000019.10:g.43768036G>A NC_000019.10:g.43768036G>C NC_000019.10:g.43768036G>T
GRCh37.p13 chr 19 NC_000019.9:g.44272188= NC_000019.9:g.44272188G>A NC_000019.9:g.44272188G>C NC_000019.9:g.44272188G>T
KCNN4 RefSeqGene (LRG_1305) NG_052672.1:g.19104= NG_052672.1:g.19104C>T NG_052672.1:g.19104C>G NG_052672.1:g.19104C>A
KCNN4 transcript NM_002250.2:c.1120-329= NM_002250.2:c.1120-329C>T NM_002250.2:c.1120-329C>G NM_002250.2:c.1120-329C>A
KCNN4 transcript NM_002250.3:c.1120-329= NM_002250.3:c.1120-329C>T NM_002250.3:c.1120-329C>G NM_002250.3:c.1120-329C>A
KCNN4 transcript variant X1 XM_005258882.1:c.1024-329= XM_005258882.1:c.1024-329C>T XM_005258882.1:c.1024-329C>G XM_005258882.1:c.1024-329C>A
KCNN4 transcript variant X1 XM_005258882.3:c.1024-329= XM_005258882.3:c.1024-329C>T XM_005258882.3:c.1024-329C>G XM_005258882.3:c.1024-329C>A
KCNN4 transcript variant X2 XM_005258883.1:c.931-329= XM_005258883.1:c.931-329C>T XM_005258883.1:c.931-329C>G XM_005258883.1:c.931-329C>A
KCNN4 transcript variant X2 XM_005258883.3:c.931-329= XM_005258883.3:c.931-329C>T XM_005258883.3:c.931-329C>G XM_005258883.3:c.931-329C>A
KCNN4 transcript variant X3 XM_005258884.1:c.724-329= XM_005258884.1:c.724-329C>T XM_005258884.1:c.724-329C>G XM_005258884.1:c.724-329C>A
KCNN4 transcript variant X4 XM_005258885.1:c.706-329= XM_005258885.1:c.706-329C>T XM_005258885.1:c.706-329C>G XM_005258885.1:c.706-329C>A
KCNN4 transcript variant X5 XM_005258886.1:c.592-329= XM_005258886.1:c.592-329C>T XM_005258886.1:c.592-329C>G XM_005258886.1:c.592-329C>A
KCNN4 transcript variant X5 XM_047438794.1:c.448-329= XM_047438794.1:c.448-329C>T XM_047438794.1:c.448-329C>G XM_047438794.1:c.448-329C>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#.

88 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss441950 Jul 12, 2000 (79)
2 SC_JCM ss735087 Aug 11, 2000 (87)
3 KWOK ss871793 Oct 04, 2000 (86)
4 KWOK ss1737765 Oct 18, 2000 (87)
5 BCM_SSAHASNP ss10926958 Jul 11, 2003 (116)
6 CSHL-HAPMAP ss20068866 Feb 27, 2004 (120)
7 SSAHASNP ss21541195 Apr 05, 2004 (121)
8 ABI ss40984959 Mar 13, 2006 (126)
9 AFFY ss66298335 Dec 02, 2006 (127)
10 AFFY ss75968347 Dec 08, 2007 (130)
11 HGSV ss78706587 Dec 06, 2007 (129)
12 KRIBB_YJKIM ss81418084 Dec 15, 2007 (130)
13 BCMHGSC_JDW ss90982435 Mar 24, 2008 (129)
14 HUMANGENOME_JCVI ss96308632 Feb 06, 2009 (130)
15 BGI ss106056432 Feb 06, 2009 (130)
16 1000GENOMES ss111406952 Jan 25, 2009 (130)
17 1000GENOMES ss115171234 Jan 25, 2009 (130)
18 ILLUMINA-UK ss117713813 Feb 14, 2009 (130)
19 ENSEMBL ss136258931 Dec 01, 2009 (131)
20 ENSEMBL ss137688799 Dec 01, 2009 (131)
21 GMI ss155925572 Dec 01, 2009 (131)
22 COMPLETE_GENOMICS ss168229355 Jul 04, 2010 (132)
23 COMPLETE_GENOMICS ss169806322 Jul 04, 2010 (132)
24 AFFY ss169806483 Jul 04, 2010 (132)
25 COMPLETE_GENOMICS ss171777405 Jul 04, 2010 (132)
26 BUSHMAN ss203762866 Jul 04, 2010 (132)
27 BCM-HGSC-SUB ss208393428 Jul 04, 2010 (132)
28 1000GENOMES ss228151883 Jul 14, 2010 (132)
29 1000GENOMES ss237686118 Jul 15, 2010 (132)
30 1000GENOMES ss243889577 Jul 15, 2010 (132)
31 BL ss255691252 May 09, 2011 (134)
32 GMI ss283219828 May 04, 2012 (137)
33 GMI ss287386427 Apr 25, 2013 (138)
34 PJP ss292182191 May 09, 2011 (134)
35 TISHKOFF ss566001634 Apr 25, 2013 (138)
36 SSMP ss661868726 Apr 25, 2013 (138)
37 EVA-GONL ss994330478 Aug 21, 2014 (142)
38 JMKIDD_LAB ss1081924027 Aug 21, 2014 (142)
39 1000GENOMES ss1363293777 Aug 21, 2014 (142)
40 DDI ss1428410985 Apr 01, 2015 (144)
41 EVA_GENOME_DK ss1578650116 Apr 01, 2015 (144)
42 EVA_UK10K_ALSPAC ss1638027015 Apr 01, 2015 (144)
43 EVA_UK10K_TWINSUK ss1681021048 Apr 01, 2015 (144)
44 EVA_DECODE ss1698385202 Apr 01, 2015 (144)
45 EVA_SVP ss1713664254 Apr 01, 2015 (144)
46 HAMMER_LAB ss1809321570 Sep 08, 2015 (146)
47 WEILL_CORNELL_DGM ss1937826220 Feb 12, 2016 (147)
48 GENOMED ss1968648699 Jul 19, 2016 (147)
49 JJLAB ss2029690768 Sep 14, 2016 (149)
50 USC_VALOUEV ss2158232632 Dec 20, 2016 (150)
51 HUMAN_LONGEVITY ss2225951673 Dec 20, 2016 (150)
52 SYSTEMSBIOZJU ss2629341673 Nov 08, 2017 (151)
53 ILLUMINA ss2635083826 Nov 08, 2017 (151)
54 GRF ss2702845269 Nov 08, 2017 (151)
55 ILLUMINA ss2710883735 Nov 08, 2017 (151)
56 GNOMAD ss2963236615 Nov 08, 2017 (151)
57 SWEGEN ss3017526151 Nov 08, 2017 (151)
58 BIOINF_KMB_FNS_UNIBA ss3028675416 Nov 08, 2017 (151)
59 CSHL ss3352316131 Nov 08, 2017 (151)
60 URBANLAB ss3650923383 Oct 12, 2018 (152)
61 EGCUT_WGS ss3684274417 Jul 13, 2019 (153)
62 EVA_DECODE ss3702828457 Jul 13, 2019 (153)
63 ACPOP ss3743064788 Jul 13, 2019 (153)
64 EVA ss3756101953 Jul 13, 2019 (153)
65 PACBIO ss3788538474 Jul 13, 2019 (153)
66 PACBIO ss3793447182 Jul 13, 2019 (153)
67 PACBIO ss3798334047 Jul 13, 2019 (153)
68 KHV_HUMAN_GENOMES ss3821349837 Jul 13, 2019 (153)
69 EVA ss3835476393 Apr 27, 2020 (154)
70 EVA ss3841360713 Apr 27, 2020 (154)
71 EVA ss3846866825 Apr 27, 2020 (154)
72 SGDP_PRJ ss3888286920 Apr 27, 2020 (154)
73 KRGDB ss3938411393 Apr 27, 2020 (154)
74 KOGIC ss3981418195 Apr 27, 2020 (154)
75 TOPMED ss5075896263 Apr 26, 2021 (155)
76 TOMMO_GENOMICS ss5227911839 Apr 26, 2021 (155)
77 1000G_HIGH_COVERAGE ss5307365073 Oct 16, 2022 (156)
78 EVA ss5435036144 Oct 16, 2022 (156)
79 HUGCELL_USP ss5499865050 Oct 16, 2022 (156)
80 1000G_HIGH_COVERAGE ss5613149147 Oct 16, 2022 (156)
81 SANFORD_IMAGENETICS ss5662457588 Oct 16, 2022 (156)
82 TOMMO_GENOMICS ss5786593955 Oct 16, 2022 (156)
83 YY_MCH ss5817629230 Oct 16, 2022 (156)
84 EVA ss5840594621 Oct 16, 2022 (156)
85 EVA ss5852300300 Oct 16, 2022 (156)
86 EVA ss5928223421 Oct 16, 2022 (156)
87 EVA ss5953867818 Oct 16, 2022 (156)
88 EVA ss5981056539 Oct 16, 2022 (156)
89 1000Genomes NC_000019.9 - 44272188 Oct 12, 2018 (152)
90 1000Genomes_30x NC_000019.10 - 43768036 Oct 16, 2022 (156)
91 The Avon Longitudinal Study of Parents and Children NC_000019.9 - 44272188 Oct 12, 2018 (152)
92 Genetic variation in the Estonian population NC_000019.9 - 44272188 Oct 12, 2018 (152)
93 The Danish reference pan genome NC_000019.9 - 44272188 Apr 27, 2020 (154)
94 gnomAD - Genomes NC_000019.10 - 43768036 Apr 26, 2021 (155)
95 Genome of the Netherlands Release 5 NC_000019.9 - 44272188 Apr 27, 2020 (154)
96 HapMap NC_000019.10 - 43768036 Apr 27, 2020 (154)
97 KOREAN population from KRGDB NC_000019.9 - 44272188 Apr 27, 2020 (154)
98 Korean Genome Project NC_000019.10 - 43768036 Apr 27, 2020 (154)
99 Northern Sweden NC_000019.9 - 44272188 Jul 13, 2019 (153)
100 Qatari NC_000019.9 - 44272188 Apr 27, 2020 (154)
101 SGDP_PRJ NC_000019.9 - 44272188 Apr 27, 2020 (154)
102 Siberian NC_000019.9 - 44272188 Apr 27, 2020 (154)
103 8.3KJPN NC_000019.9 - 44272188 Apr 26, 2021 (155)
104 14KJPN NC_000019.10 - 43768036 Oct 16, 2022 (156)
105 TopMed NC_000019.10 - 43768036 Apr 26, 2021 (155)
106 UK 10K study - Twins NC_000019.9 - 44272188 Oct 12, 2018 (152)
107 A Vietnamese Genetic Variation Database NC_000019.9 - 44272188 Jul 13, 2019 (153)
108 ALFA NC_000019.10 - 43768036 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)
rs563912 Oct 23, 2000 (87)
rs56437932 May 26, 2008 (130)
rs59301188 Feb 27, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss66298335, ss75968347, ss78706587, ss90982435, ss111406952, ss115171234, ss117713813, ss168229355, ss169806322, ss169806483, ss171777405, ss203762866, ss208393428, ss255691252, ss283219828, ss287386427, ss292182191, ss1698385202, ss1713664254, ss2635083826 NC_000019.8:48964027:G:A NC_000019.10:43768035:G:A (self)
76704871, 42475123, 30012665, 4832130, 18922295, 45588787, 16349653, 19868142, 40303900, 10748986, 85881146, 42475123, 9379614, ss228151883, ss237686118, ss243889577, ss566001634, ss661868726, ss994330478, ss1081924027, ss1363293777, ss1428410985, ss1578650116, ss1638027015, ss1681021048, ss1809321570, ss1937826220, ss1968648699, ss2029690768, ss2158232632, ss2629341673, ss2702845269, ss2710883735, ss2963236615, ss3017526151, ss3352316131, ss3684274417, ss3743064788, ss3756101953, ss3788538474, ss3793447182, ss3798334047, ss3835476393, ss3841360713, ss3888286920, ss3938411393, ss5227911839, ss5435036144, ss5662457588, ss5840594621, ss5953867818, ss5981056539 NC_000019.9:44272187:G:A NC_000019.10:43768035:G:A (self)
100675082, 540962355, 1700105, 37796196, 120431059, 291441927, 7463196109, ss2225951673, ss3028675416, ss3650923383, ss3702828457, ss3821349837, ss3846866825, ss3981418195, ss5075896263, ss5307365073, ss5499865050, ss5613149147, ss5786593955, ss5817629230, ss5852300300, ss5928223421 NC_000019.10:43768035:G:A NC_000019.10:43768035:G:A (self)
ss10926958, ss20068866, ss21541195 NT_011109.15:16540405:G:A NC_000019.10:43768035:G:A (self)
ss441950, ss735087, ss871793, ss1737765, ss40984959, ss81418084, ss96308632, ss106056432, ss136258931, ss137688799, ss155925572 NT_011109.16:16540405:G:A NC_000019.10:43768035:G:A (self)
45588787, ss3938411393 NC_000019.9:44272187:G:C NC_000019.10:43768035:G:C (self)
45588787, ss3938411393 NC_000019.9:44272187:G:T NC_000019.10:43768035: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.

No publications for rs347518

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