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rs121912243

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912243(C;T)
Make rs121912243(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63350969
GeneCHRNA4
is asnp
is mentioned by
dbSNPrs121912243
ebirs121912243
HLIrs121912243
Exacrs121912243
Varsomers121912243
Maprs121912243
PheGenIrs121912243
hapmaprs121912243
1000 genomesrs121912243
hgdprs121912243
ensemblrs121912243
gopubmedrs121912243
geneviewrs121912243
scholarrs121912243
googlers121912243
pharmgkbrs121912243
gwascentralrs121912243
openSNPrs121912243
23andMers121912243
23andMe allrs121912243
SNP Nexus

SNPshotrs121912243
SNPdbers121912243
MSV3drs121912243
GWAS Ctlgrs121912243
Max Magnitude0
ClinVar
Risk rs121912243(T;T)
Alt rs121912243(T;T)
Reference rs121912243(C;C)
Significance Probable-Pathogenic
Disease Tobacco use disorder not specified Inborn genetic diseases
Variation info
Gene CHRNA4
CLNDBN Tobacco use disorder not specified Inborn genetic diseases
Reversed 1
HGVS NC_000020.10:g.61982321G>A
CLNSRC
CLNACC RCV000084614.1, RCV000186922.2, RCV000190688.1,