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rs794728831

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728831(A;A)
Make rs794728831(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237806263
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728831
ebirs794728831
HLIrs794728831
Exacrs794728831
Varsomers794728831
Maprs794728831
PheGenIrs794728831
hapmaprs794728831
1000 genomesrs794728831
hgdprs794728831
ensemblrs794728831
gopubmedrs794728831
geneviewrs794728831
scholarrs794728831
googlers794728831
pharmgkbrs794728831
gwascentralrs794728831
openSNPrs794728831
23andMers794728831
23andMe allrs794728831
SNP Nexus

SNPshotrs794728831
SNPdbers794728831
MSV3drs794728831
GWAS Ctlgrs794728831
Max Magnitude0
ClinVar
Risk rs794728831(A;A)
Alt rs794728831(A;A)
Reference rs794728831(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237969563G>A
CLNSRC
CLNACC RCV000182894.1,