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rs199473657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473657(G;T)
Make rs199473657(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175718
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473657
dbSNP (classic)rs199473657
ClinGenrs199473657
ebirs199473657
HLIrs199473657
Exacrs199473657
Gnomadrs199473657
Varsomers199473657
LitVarrs199473657
Maprs199473657
PheGenIrs199473657
Biobankrs199473657
1000 genomesrs199473657
hgdprs199473657
ensemblrs199473657
geneviewrs199473657
scholarrs199473657
googlers199473657
pharmgkbrs199473657
gwascentralrs199473657
openSNPrs199473657
23andMers199473657
SNPshotrs199473657
SNPdbers199473657
MSV3drs199473657
GWAS Ctlgrs199473657
Max Magnitude0
ClinVar
Risk rs199473657(T;T)
Alt rs199473657(T;T)
Reference Rs199473657(G;G)
Significance Untested
Disease Ventricular tachycardia
Variation info
Gene KCNJ2
CLNDBN Ventricular tachycardia
Reversed 0
HGVS NC_000017.10:g.68171859G>T
CLNSRC ClinVar
CLNACC RCV000058328.3,