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rs794728746

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728746(C;C)
Make rs794728746(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237638480
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728746
ebirs794728746
HLIrs794728746
Exacrs794728746
Varsomers794728746
Maprs794728746
PheGenIrs794728746
hapmaprs794728746
1000 genomesrs794728746
hgdprs794728746
ensemblrs794728746
gopubmedrs794728746
geneviewrs794728746
scholarrs794728746
googlers794728746
pharmgkbrs794728746
gwascentralrs794728746
openSNPrs794728746
23andMers794728746
23andMe allrs794728746
SNP Nexus

SNPshotrs794728746
SNPdbers794728746
MSV3drs794728746
GWAS Ctlgrs794728746
Max Magnitude0
ClinVar
Risk rs794728746(A,C;A,C)
Alt rs794728746(A,C;A,C)
Reference rs794728746(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.237801780G>A; NC_000001.10:g.237801780G>C
CLNSRC
CLNACC RCV000182876.1, RCV000226725.1, RCV000182748.1,