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rs786205273

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205273(-;-)
Make rs786205273(-;G)
Make rs786205273(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237614785
GeneRYR2
is asnp
is mentioned by
dbSNPrs786205273
ebirs786205273
HLIrs786205273
Exacrs786205273
Varsomers786205273
Maprs786205273
PheGenIrs786205273
hapmaprs786205273
1000 genomesrs786205273
hgdprs786205273
ensemblrs786205273
gopubmedrs786205273
geneviewrs786205273
scholarrs786205273
googlers786205273
pharmgkbrs786205273
gwascentralrs786205273
openSNPrs786205273
23andMers786205273
23andMe allrs786205273
SNP Nexus

SNPshotrs786205273
SNPdbers786205273
MSV3drs786205273
GWAS Ctlgrs786205273
Max Magnitude0
ClinVar
Risk rs786205273(G;G)
Alt rs786205273(G;G)
Reference rs786205273(;)
Significance Probable-Pathogenic
Disease Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN Ventricular tachycardia, polymorphic
Reversed 0
HGVS NC_000001.10:g.237778085dupG
CLNSRC
CLNACC RCV000171566.1,