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rs794728756

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728756(A;A)
Make rs794728756(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237640983
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728756
ebirs794728756
HLIrs794728756
Exacrs794728756
Varsomers794728756
Maprs794728756
PheGenIrs794728756
hapmaprs794728756
1000 genomesrs794728756
hgdprs794728756
ensemblrs794728756
gopubmedrs794728756
geneviewrs794728756
scholarrs794728756
googlers794728756
pharmgkbrs794728756
gwascentralrs794728756
openSNPrs794728756
23andMers794728756
23andMe allrs794728756
SNP Nexus

SNPshotrs794728756
SNPdbers794728756
MSV3drs794728756
GWAS Ctlgrs794728756
Max Magnitude0
ClinVar
Risk rs794728756(A,T;A,T)
Alt rs794728756(A,T;A,T)
Reference rs794728756(G;G)
Significance Pathogenic
Disease not provided Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN not provided Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.237804283G>A; NC_000001.10:g.237804283G>T
CLNSRC
CLNACC RCV000182760.1, RCV000208074.1, RCV000182761.1,