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rs199473533

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473533(A;T)
Make rs199473533(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150950384
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473533
ebirs199473533
HLIrs199473533
Exacrs199473533
Varsomers199473533
Maprs199473533
PheGenIrs199473533
hapmaprs199473533
1000 genomesrs199473533
hgdprs199473533
ensemblrs199473533
gopubmedrs199473533
geneviewrs199473533
scholarrs199473533
googlers199473533
pharmgkbrs199473533
gwascentralrs199473533
openSNPrs199473533
23andMers199473533
23andMe allrs199473533
SNP Nexus

SNPshotrs199473533
SNPdbers199473533
MSV3drs199473533
GWAS Ctlgrs199473533
Max Magnitude0
ClinVar
Risk rs199473533(T;T)
Alt rs199473533(T;T)
Reference rs199473533(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.150647472T>A
CLNSRC ClinVar
CLNACC RCV000058093.2,