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rs794728775

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728775(A;A)
Make rs794728775(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237772042
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728775
ebirs794728775
HLIrs794728775
Exacrs794728775
Varsomers794728775
Maprs794728775
PheGenIrs794728775
hapmaprs794728775
1000 genomesrs794728775
hgdprs794728775
ensemblrs794728775
gopubmedrs794728775
geneviewrs794728775
scholarrs794728775
googlers794728775
pharmgkbrs794728775
gwascentralrs794728775
openSNPrs794728775
23andMers794728775
23andMe allrs794728775
SNP Nexus

SNPshotrs794728775
SNPdbers794728775
MSV3drs794728775
GWAS Ctlgrs794728775
Max Magnitude0
ClinVar
Risk rs794728775(A;A)
Alt rs794728775(A;A)
Reference rs794728775(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237935342G>A
CLNSRC
CLNACC RCV000182798.2,