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rs199473373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473373(C;T)
Make rs199473373(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175283
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473373
ebirs199473373
HLIrs199473373
Exacrs199473373
Varsomers199473373
Maprs199473373
PheGenIrs199473373
hapmaprs199473373
1000 genomesrs199473373
hgdprs199473373
ensemblrs199473373
gopubmedrs199473373
geneviewrs199473373
scholarrs199473373
googlers199473373
pharmgkbrs199473373
gwascentralrs199473373
openSNPrs199473373
23andMers199473373
23andMe allrs199473373
SNP Nexus

SNPshotrs199473373
SNPdbers199473373
MSV3drs199473373
GWAS Ctlgrs199473373
Max Magnitude0
ClinVar
Risk rs199473373(T;T)
Alt rs199473373(T;T)
Reference rs199473373(C;C)
Significance Pathogenic
Disease Ventricular tachycardia not provided
Variation info
Gene KCNJ2
CLNDBN Ventricular tachycardia not provided
Reversed 0
HGVS NC_000017.10:g.68171424C>T
CLNSRC ClinVar
CLNACC RCV000058305.2, RCV000170976.3,