Have questions? Visit https://www.reddit.com/r/SNPedia

rs199472889

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472889(A;T)
Make rs199472889(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150957394
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472889
ebirs199472889
HLIrs199472889
Exacrs199472889
Varsomers199472889
Maprs199472889
PheGenIrs199472889
hapmaprs199472889
1000 genomesrs199472889
hgdprs199472889
ensemblrs199472889
gopubmedrs199472889
geneviewrs199472889
scholarrs199472889
googlers199472889
pharmgkbrs199472889
gwascentralrs199472889
openSNPrs199472889
23andMers199472889
23andMe allrs199472889
SNP Nexus

SNPshotrs199472889
SNPdbers199472889
MSV3drs199472889
GWAS Ctlgrs199472889
Max Magnitude0
ClinVar
Risk rs199472889(C,T;C,T)
Alt rs199472889(C,T;C,T)
Reference rs199472889(A;A)
Significance Pathogenic
Disease Acquired long QT syndrome
Variation info
Gene KCNH2
CLNDBN Acquired long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150654482T>A
CLNSRC ClinVar
CLNACC RCV000057869.2,