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rs794728706

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728706(A;G)
Make rs794728706(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237330948
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728706
ebirs794728706
HLIrs794728706
Exacrs794728706
Varsomers794728706
Maprs794728706
PheGenIrs794728706
hapmaprs794728706
1000 genomesrs794728706
hgdprs794728706
ensemblrs794728706
gopubmedrs794728706
geneviewrs794728706
scholarrs794728706
googlers794728706
pharmgkbrs794728706
gwascentralrs794728706
openSNPrs794728706
23andMers794728706
23andMe allrs794728706
SNP Nexus

SNPshotrs794728706
SNPdbers794728706
MSV3drs794728706
GWAS Ctlgrs794728706
Max Magnitude0
ClinVar
Risk rs794728706(G;G)
Alt rs794728706(G;G)
Reference rs794728706(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237494248A>G
CLNSRC
CLNACC RCV000182653.1,