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rs199472934

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472934(A;G)
Make rs199472934(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951603
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472934
ebirs199472934
HLIrs199472934
Exacrs199472934
Varsomers199472934
Maprs199472934
PheGenIrs199472934
hapmaprs199472934
1000 genomesrs199472934
hgdprs199472934
ensemblrs199472934
gopubmedrs199472934
geneviewrs199472934
scholarrs199472934
googlers199472934
pharmgkbrs199472934
gwascentralrs199472934
openSNPrs199472934
23andMers199472934
23andMe allrs199472934
SNP Nexus

SNPshotrs199472934
SNPdbers199472934
MSV3drs199472934
GWAS Ctlgrs199472934
Max Magnitude0
ClinVar
Risk rs199472934(G;G)
Alt rs199472934(G;G)
Reference rs199472934(A;A)
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.150648691T>C
CLNSRC ClinVar
CLNACC RCV000057993.2, RCV000168208.2,