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rs199473374

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473374(C;C)
Make rs199473374(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175340
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473374
ebirs199473374
HLIrs199473374
Exacrs199473374
Varsomers199473374
Maprs199473374
PheGenIrs199473374
hapmaprs199473374
1000 genomesrs199473374
hgdprs199473374
ensemblrs199473374
gopubmedrs199473374
geneviewrs199473374
scholarrs199473374
googlers199473374
pharmgkbrs199473374
gwascentralrs199473374
openSNPrs199473374
23andMers199473374
23andMe allrs199473374
SNP Nexus

SNPshotrs199473374
SNPdbers199473374
MSV3drs199473374
GWAS Ctlgrs199473374
Max Magnitude0
ClinVar
Risk rs199473374(C;C)
Alt rs199473374(C;C)
Reference rs199473374(T;T)
Significance Pathogenic
Disease Ventricular tachycardia
Variation info
Gene KCNJ2
CLNDBN Ventricular tachycardia
Reversed 0
HGVS NC_000017.10:g.68171481T>C
CLNSRC ClinVar
CLNACC RCV000058308.2,