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rs199472981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472981(C;C)
Make rs199472981(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951033
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472981
ebirs199472981
HLIrs199472981
Exacrs199472981
Varsomers199472981
Maprs199472981
PheGenIrs199472981
hapmaprs199472981
1000 genomesrs199472981
hgdprs199472981
ensemblrs199472981
gopubmedrs199472981
geneviewrs199472981
scholarrs199472981
googlers199472981
pharmgkbrs199472981
gwascentralrs199472981
openSNPrs199472981
23andMers199472981
23andMe allrs199472981
SNP Nexus

SNPshotrs199472981
SNPdbers199472981
MSV3drs199472981
GWAS Ctlgrs199472981
Max Magnitude0
ClinVar
Risk rs199472981(C;C)
Alt rs199472981(C;C)
Reference rs199472981(T;T)
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.150648121A>G
CLNSRC ClinVar
CLNACC RCV000058076.2, RCV000232888.1,