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rs199472909

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472909(A;T)
Make rs199472909(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952517
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472909
ebirs199472909
HLIrs199472909
Exacrs199472909
Varsomers199472909
Maprs199472909
PheGenIrs199472909
hapmaprs199472909
1000 genomesrs199472909
hgdprs199472909
ensemblrs199472909
gopubmedrs199472909
geneviewrs199472909
scholarrs199472909
googlers199472909
pharmgkbrs199472909
gwascentralrs199472909
openSNPrs199472909
23andMers199472909
23andMe allrs199472909
SNP Nexus

SNPshotrs199472909
SNPdbers199472909
MSV3drs199472909
GWAS Ctlgrs199472909
Max Magnitude0
ClinVar
Risk rs199472909(T;T)
Alt rs199472909(T;T)
Reference rs199472909(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649605T>A
CLNSRC ClinVar
CLNACC RCV000057909.2,