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rs199472841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472841(G;T)
Make rs199472841(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974868
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472841
ebirs199472841
HLIrs199472841
Exacrs199472841
Varsomers199472841
Maprs199472841
PheGenIrs199472841
hapmaprs199472841
1000 genomesrs199472841
hgdprs199472841
ensemblrs199472841
gopubmedrs199472841
geneviewrs199472841
scholarrs199472841
googlers199472841
pharmgkbrs199472841
gwascentralrs199472841
openSNPrs199472841
23andMers199472841
23andMe allrs199472841
SNP Nexus

SNPshotrs199472841
SNPdbers199472841
MSV3drs199472841
GWAS Ctlgrs199472841
Max Magnitude0
ClinVar
Risk rs199472841(T;T)
Alt rs199472841(T;T)
Reference rs199472841(G;G)
Significance Pathogenic
Disease short QT syndrome
Variation info
Gene KCNH2
CLNDBN short QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671956C>A
CLNSRC ClinVar
CLNACC RCV000057920.2,