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rs199472924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472924(C;C)
Make rs199472924(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951702
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472924
ebirs199472924
HLIrs199472924
Exacrs199472924
Varsomers199472924
Maprs199472924
PheGenIrs199472924
hapmaprs199472924
1000 genomesrs199472924
hgdprs199472924
ensemblrs199472924
gopubmedrs199472924
geneviewrs199472924
scholarrs199472924
googlers199472924
pharmgkbrs199472924
gwascentralrs199472924
openSNPrs199472924
23andMers199472924
23andMe allrs199472924
SNP Nexus

SNPshotrs199472924
SNPdbers199472924
MSV3drs199472924
GWAS Ctlgrs199472924
Max Magnitude0
ClinVar
Risk rs199472924(C;C)
Alt rs199472924(C;C)
Reference rs199472924(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648790A>G
CLNSRC ClinVar
CLNACC RCV000057946.2,