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rs199473026

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473026(C;C)
Make rs199473026(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947334
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473026
ebirs199473026
HLIrs199473026
Exacrs199473026
Varsomers199473026
Maprs199473026
PheGenIrs199473026
hapmaprs199473026
1000 genomesrs199473026
hgdprs199473026
ensemblrs199473026
gopubmedrs199473026
geneviewrs199473026
scholarrs199473026
googlers199473026
pharmgkbrs199473026
gwascentralrs199473026
openSNPrs199473026
23andMers199473026
23andMe allrs199473026
SNP Nexus

SNPshotrs199473026
SNPdbers199473026
MSV3drs199473026
GWAS Ctlgrs199473026
Max Magnitude0
ClinVar
Risk rs199473026(C;C)
Alt rs199473026(C;C)
Reference rs199473026(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.150644422A>G
CLNSRC ClinVar
CLNACC RCV000058203.2,