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rs199473536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473536(A;A)
Make rs199473536(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150949049
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473536
ebirs199473536
HLIrs199473536
Exacrs199473536
Varsomers199473536
Maprs199473536
PheGenIrs199473536
hapmaprs199473536
1000 genomesrs199473536
hgdprs199473536
ensemblrs199473536
gopubmedrs199473536
geneviewrs199473536
scholarrs199473536
googlers199473536
pharmgkbrs199473536
gwascentralrs199473536
openSNPrs199473536
23andMers199473536
23andMe allrs199473536
SNP Nexus

SNPshotrs199473536
SNPdbers199473536
MSV3drs199473536
GWAS Ctlgrs199473536
Max Magnitude0
ClinVar
Risk rs199473536(A;A)
Alt rs199473536(A;A)
Reference rs199473536(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150646137C>T
CLNSRC ClinVar
CLNACC RCV000058116.2,