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rs199472932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472932(A;G)
Make rs199472932(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951610
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472932
ebirs199472932
HLIrs199472932
Exacrs199472932
Varsomers199472932
Maprs199472932
PheGenIrs199472932
hapmaprs199472932
1000 genomesrs199472932
hgdprs199472932
ensemblrs199472932
gopubmedrs199472932
geneviewrs199472932
scholarrs199472932
googlers199472932
pharmgkbrs199472932
gwascentralrs199472932
openSNPrs199472932
23andMers199472932
23andMe allrs199472932
SNP Nexus

SNPshotrs199472932
SNPdbers199472932
MSV3drs199472932
GWAS Ctlgrs199472932
Max Magnitude0
ClinVar
Risk rs199472932(G;G)
Alt rs199472932(G;G)
Reference rs199472932(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648698T>C
CLNSRC ClinVar
CLNACC RCV000057988.2,