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rs199473032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473032(C;T)
Make rs199473032(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150945498
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473032
ebirs199473032
HLIrs199473032
Exacrs199473032
Varsomers199473032
Maprs199473032
PheGenIrs199473032
hapmaprs199473032
1000 genomesrs199473032
hgdprs199473032
ensemblrs199473032
gopubmedrs199473032
geneviewrs199473032
scholarrs199473032
googlers199473032
pharmgkbrs199473032
gwascentralrs199473032
openSNPrs199473032
23andMers199473032
23andMe allrs199473032
SNP Nexus

SNPshotrs199473032
SNPdbers199473032
MSV3drs199473032
GWAS Ctlgrs199473032
Max Magnitude0
ClinVar
Risk rs199473032(T;T)
Alt rs199473032(T;T)
Reference rs199473032(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150642586G>A
CLNSRC ClinVar
CLNACC RCV000058220.2,