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rs199472923

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472923(G;G)
Make rs199472923(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951706
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472923
ebirs199472923
HLIrs199472923
Exacrs199472923
Varsomers199472923
Maprs199472923
PheGenIrs199472923
hapmaprs199472923
1000 genomesrs199472923
hgdprs199472923
ensemblrs199472923
gopubmedrs199472923
geneviewrs199472923
scholarrs199472923
googlers199472923
pharmgkbrs199472923
gwascentralrs199472923
openSNPrs199472923
23andMers199472923
23andMe allrs199472923
SNP Nexus

SNPshotrs199472923
SNPdbers199472923
MSV3drs199472923
GWAS Ctlgrs199472923
Max Magnitude0
ClinVar
Risk rs199472923(G;G)
Alt rs199472923(G;G)
Reference rs199472923(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.150648794A>C
CLNSRC ClinVar
CLNACC RCV000057944.2,