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rs199473665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473665(C;C)
Make rs199473665(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974812
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473665
ebirs199473665
HLIrs199473665
Exacrs199473665
Varsomers199473665
Maprs199473665
PheGenIrs199473665
hapmaprs199473665
1000 genomesrs199473665
hgdprs199473665
ensemblrs199473665
gopubmedrs199473665
geneviewrs199473665
scholarrs199473665
googlers199473665
pharmgkbrs199473665
gwascentralrs199473665
openSNPrs199473665
23andMers199473665
23andMe allrs199473665
SNP Nexus

SNPshotrs199473665
SNPdbers199473665
MSV3drs199473665
GWAS Ctlgrs199473665
Max Magnitude0
ClinVar
Risk rs199473665(C;C)
Alt rs199473665(C;C)
Reference rs199473665(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.150671900A>G
CLNSRC ClinVar
CLNACC RCV000058078.2,