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rs794728778

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728778(A;A)
Make rs794728778(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237781643
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728778
ebirs794728778
HLIrs794728778
Exacrs794728778
Varsomers794728778
Maprs794728778
PheGenIrs794728778
hapmaprs794728778
1000 genomesrs794728778
hgdprs794728778
ensemblrs794728778
gopubmedrs794728778
geneviewrs794728778
scholarrs794728778
googlers794728778
pharmgkbrs794728778
gwascentralrs794728778
openSNPrs794728778
23andMers794728778
23andMe allrs794728778
SNP Nexus

SNPshotrs794728778
SNPdbers794728778
MSV3drs794728778
GWAS Ctlgrs794728778
Max Magnitude0
ClinVar
Risk rs794728778(A;A)
Alt rs794728778(A;A)
Reference rs794728778(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237944943G>A
CLNSRC
CLNACC RCV000182802.1,