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rs199472826

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472826(C;C)
Make rs199472826(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150977849
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472826
ebirs199472826
HLIrs199472826
Exacrs199472826
Varsomers199472826
Maprs199472826
PheGenIrs199472826
hapmaprs199472826
1000 genomesrs199472826
hgdprs199472826
ensemblrs199472826
gopubmedrs199472826
geneviewrs199472826
scholarrs199472826
googlers199472826
pharmgkbrs199472826
gwascentralrs199472826
openSNPrs199472826
23andMers199472826
23andMe allrs199472826
SNP Nexus

SNPshotrs199472826
SNPdbers199472826
MSV3drs199472826
GWAS Ctlgrs199472826
Max Magnitude0
ClinVar
Risk rs199472826(C;C)
Alt rs199472826(C;C)
Reference rs199472826(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.150674937A>G
CLNSRC ClinVar
CLNACC RCV000058246.2,