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rs794728776

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728776(A;G)
Make rs794728776(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237772045
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728776
ebirs794728776
HLIrs794728776
Exacrs794728776
Varsomers794728776
Maprs794728776
PheGenIrs794728776
hapmaprs794728776
1000 genomesrs794728776
hgdprs794728776
ensemblrs794728776
gopubmedrs794728776
geneviewrs794728776
scholarrs794728776
googlers794728776
pharmgkbrs794728776
gwascentralrs794728776
openSNPrs794728776
23andMers794728776
23andMe allrs794728776
SNP Nexus

SNPshotrs794728776
SNPdbers794728776
MSV3drs794728776
GWAS Ctlgrs794728776
Max Magnitude0
ClinVar
Risk rs794728776(G;G)
Alt rs794728776(G;G)
Reference rs794728776(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene RYR2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.237935345A>G
CLNSRC
CLNACC RCV000223705.1,