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rs794728753

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728753(A;A)
Make rs794728753(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237640940
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728753
ebirs794728753
HLIrs794728753
Exacrs794728753
Varsomers794728753
Maprs794728753
PheGenIrs794728753
hapmaprs794728753
1000 genomesrs794728753
hgdprs794728753
ensemblrs794728753
gopubmedrs794728753
geneviewrs794728753
scholarrs794728753
googlers794728753
pharmgkbrs794728753
gwascentralrs794728753
openSNPrs794728753
23andMers794728753
23andMe allrs794728753
SNP Nexus

SNPshotrs794728753
SNPdbers794728753
MSV3drs794728753
GWAS Ctlgrs794728753
Max Magnitude0
ClinVar
Risk rs794728753(A;A)
Alt rs794728753(A;A)
Reference rs794728753(G;G)
Significance Pathogenic
Disease not provided Catecholaminergic polymorphic ventricular tachycardia
Variation info
Gene RYR2
CLNDBN not provided Catecholaminergic polymorphic ventricular tachycardia
Reversed 0
HGVS NC_000001.10:g.237804240G>A
CLNSRC
CLNACC RCV000182757.2, RCV000217048.1,