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rs199472984

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472984(C;T)
Make rs199472984(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150950980
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472984
ebirs199472984
HLIrs199472984
Exacrs199472984
Varsomers199472984
Maprs199472984
PheGenIrs199472984
hapmaprs199472984
1000 genomesrs199472984
hgdprs199472984
ensemblrs199472984
gopubmedrs199472984
geneviewrs199472984
scholarrs199472984
googlers199472984
pharmgkbrs199472984
gwascentralrs199472984
openSNPrs199472984
23andMers199472984
23andMe allrs199472984
SNP Nexus

SNPshotrs199472984
SNPdbers199472984
MSV3drs199472984
GWAS Ctlgrs199472984
Max Magnitude0
ClinVar
Risk rs199472984(T;T)
Alt rs199472984(T;T)
Reference rs199472984(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648068G>A
CLNSRC ClinVar
CLNACC RCV000058080.2,