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rs794728811

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728811(A;A)
Make rs794728811(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237832619
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728811
ebirs794728811
HLIrs794728811
Exacrs794728811
Varsomers794728811
Maprs794728811
PheGenIrs794728811
hapmaprs794728811
1000 genomesrs794728811
hgdprs794728811
ensemblrs794728811
gopubmedrs794728811
geneviewrs794728811
scholarrs794728811
googlers794728811
pharmgkbrs794728811
gwascentralrs794728811
openSNPrs794728811
23andMers794728811
23andMe allrs794728811
SNP Nexus

SNPshotrs794728811
SNPdbers794728811
MSV3drs794728811
GWAS Ctlgrs794728811
Max Magnitude0
ClinVar
Risk rs794728811(A;A)
Alt rs794728811(A;A)
Reference rs794728811(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237995919G>A
CLNSRC
CLNACC RCV000182854.1,