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rs199473435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473435(C;T)
Make rs199473435(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947854
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473435
ebirs199473435
HLIrs199473435
Exacrs199473435
Varsomers199473435
Maprs199473435
PheGenIrs199473435
hapmaprs199473435
1000 genomesrs199473435
hgdprs199473435
ensemblrs199473435
gopubmedrs199473435
geneviewrs199473435
scholarrs199473435
googlers199473435
pharmgkbrs199473435
gwascentralrs199473435
openSNPrs199473435
23andMers199473435
23andMe allrs199473435
SNP Nexus

SNPshotrs199473435
SNPdbers199473435
MSV3drs199473435
GWAS Ctlgrs199473435
Max Magnitude0
ClinVar
Risk rs199473435(T;T)
Alt rs199473435(T;T)
Reference rs199473435(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644942G>A
CLNSRC ClinVar
CLNACC RCV000058154.2, RCV000203863.2,