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rs199473431

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473431(A;G)
Make rs199473431(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951631
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473431
ebirs199473431
HLIrs199473431
Exacrs199473431
Varsomers199473431
Maprs199473431
PheGenIrs199473431
hapmaprs199473431
1000 genomesrs199473431
hgdprs199473431
ensemblrs199473431
gopubmedrs199473431
geneviewrs199473431
scholarrs199473431
googlers199473431
pharmgkbrs199473431
gwascentralrs199473431
openSNPrs199473431
23andMers199473431
23andMe allrs199473431
SNP Nexus

SNPshotrs199473431
SNPdbers199473431
MSV3drs199473431
GWAS Ctlgrs199473431
Max Magnitude0
ClinVar
Risk rs199473431(G;G)
Alt rs199473431(G;G)
Reference rs199473431(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.150648719T>C
CLNSRC ClinVar
CLNACC RCV000057979.2,