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rs199473534

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473534(A;G)
Make rs199473534(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150950300
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473534
ebirs199473534
HLIrs199473534
Exacrs199473534
Varsomers199473534
Maprs199473534
PheGenIrs199473534
hapmaprs199473534
1000 genomesrs199473534
hgdprs199473534
ensemblrs199473534
gopubmedrs199473534
geneviewrs199473534
scholarrs199473534
googlers199473534
pharmgkbrs199473534
gwascentralrs199473534
openSNPrs199473534
23andMers199473534
23andMe allrs199473534
SNP Nexus

SNPshotrs199473534
SNPdbers199473534
MSV3drs199473534
GWAS Ctlgrs199473534
Max Magnitude0
ClinVar
Risk rs199473534(G;G)
Alt rs199473534(G;G)
Reference rs199473534(A;A)
Significance Pathogenic
Disease Acquired long QT syndrome
Variation info
Gene KCNH2
CLNDBN Acquired long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150647388T>C
CLNSRC ClinVar
CLNACC RCV000058102.2,