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rs199473493

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473493(C;T)
Make rs199473493(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974779
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473493
ebirs199473493
HLIrs199473493
Exacrs199473493
Varsomers199473493
Maprs199473493
PheGenIrs199473493
hapmaprs199473493
1000 genomesrs199473493
hgdprs199473493
ensemblrs199473493
gopubmedrs199473493
geneviewrs199473493
scholarrs199473493
googlers199473493
pharmgkbrs199473493
gwascentralrs199473493
openSNPrs199473493
23andMers199473493
23andMe allrs199473493
SNP Nexus

SNPshotrs199473493
SNPdbers199473493
MSV3drs199473493
GWAS Ctlgrs199473493
Max Magnitude0
ClinVar
Risk rs199473493(T;T)
Alt rs199473493(T;T)
Reference rs199473493(C;C)
Significance Pathogenic
Disease Sudden cardiac death
Variation info
Gene KCNH2
CLNDBN Sudden cardiac death
Reversed 1
HGVS NC_000007.13:g.150671867G>A
CLNSRC ClinVar
CLNACC RCV000058117.2,