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rs794728709

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728709(A;A)
Make rs794728709(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237377394
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728709
ebirs794728709
HLIrs794728709
Exacrs794728709
Varsomers794728709
Maprs794728709
PheGenIrs794728709
hapmaprs794728709
1000 genomesrs794728709
hgdprs794728709
ensemblrs794728709
gopubmedrs794728709
geneviewrs794728709
scholarrs794728709
googlers794728709
pharmgkbrs794728709
gwascentralrs794728709
openSNPrs794728709
23andMers794728709
23andMe allrs794728709
SNP Nexus

SNPshotrs794728709
SNPdbers794728709
MSV3drs794728709
GWAS Ctlgrs794728709
Max Magnitude0
ClinVar
Risk rs794728709(A;A)
Alt rs794728709(A;A)
Reference rs794728709(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237540694G>A
CLNSRC
CLNACC RCV000182661.1,