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rs373394254

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373394254(A;A)
Make rs373394254(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947386
GeneKCNH2
is asnp
is mentioned by
dbSNPrs373394254
ebirs373394254
HLIrs373394254
Exacrs373394254
Varsomers373394254
Maprs373394254
PheGenIrs373394254
hapmaprs373394254
1000 genomesrs373394254
hgdprs373394254
ensemblrs373394254
gopubmedrs373394254
geneviewrs373394254
scholarrs373394254
googlers373394254
pharmgkbrs373394254
gwascentralrs373394254
openSNPrs373394254
23andMers373394254
23andMe allrs373394254
SNP Nexus

SNPshotrs373394254
SNPdbers373394254
MSV3drs373394254
GWAS Ctlgrs373394254
Max Magnitude0
ClinVar
Risk rs373394254(A;A)
Alt rs373394254(A;A)
Reference rs373394254(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000007.13:g.150644474G>A
CLNSRC
CLNACC RCV000181909.1,