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rs199472858

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472858(A;A)
Make rs199472858(A;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959727
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472858
ebirs199472858
HLIrs199472858
Exacrs199472858
Varsomers199472858
Maprs199472858
PheGenIrs199472858
hapmaprs199472858
1000 genomesrs199472858
hgdprs199472858
ensemblrs199472858
gopubmedrs199472858
geneviewrs199472858
scholarrs199472858
googlers199472858
pharmgkbrs199472858
gwascentralrs199472858
openSNPrs199472858
23andMers199472858
23andMe allrs199472858
SNP Nexus

SNPshotrs199472858
SNPdbers199472858
MSV3drs199472858
GWAS Ctlgrs199472858
Max Magnitude0
ClinVar
Risk rs199472858(A;A)
Alt rs199472858(A;A)
Reference rs199472858(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150656815A>T
CLNSRC ClinVar
CLNACC RCV000058206.2,