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rs199473424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473424(A;G)
Make rs199473424(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951669
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473424
ebirs199473424
HLIrs199473424
Exacrs199473424
Varsomers199473424
Maprs199473424
PheGenIrs199473424
hapmaprs199473424
1000 genomesrs199473424
hgdprs199473424
ensemblrs199473424
gopubmedrs199473424
geneviewrs199473424
scholarrs199473424
googlers199473424
pharmgkbrs199473424
gwascentralrs199473424
openSNPrs199473424
23andMers199473424
23andMe allrs199473424
SNP Nexus

SNPshotrs199473424
SNPdbers199473424
MSV3drs199473424
GWAS Ctlgrs199473424
Max Magnitude0
ClinVar
Risk rs199473424(G;G)
Alt rs199473424(G;G)
Reference rs199473424(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.150648757T>C
CLNSRC ClinVar
CLNACC RCV000057965.2,