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rs794728807

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728807(A;A)
Make rs794728807(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237830569
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728807
ebirs794728807
HLIrs794728807
Exacrs794728807
Varsomers794728807
Maprs794728807
PheGenIrs794728807
hapmaprs794728807
1000 genomesrs794728807
hgdprs794728807
ensemblrs794728807
gopubmedrs794728807
geneviewrs794728807
scholarrs794728807
googlers794728807
pharmgkbrs794728807
gwascentralrs794728807
openSNPrs794728807
23andMers794728807
23andMe allrs794728807
SNP Nexus

SNPshotrs794728807
SNPdbers794728807
MSV3drs794728807
GWAS Ctlgrs794728807
Max Magnitude0
ClinVar
Risk rs794728807(A;A)
Alt rs794728807(A;A)
Reference rs794728807(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237993869G>A
CLNSRC
CLNACC RCV000182849.2,