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rs794728791

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728791(A;A)
Make rs794728791(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784295
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728791
ebirs794728791
HLIrs794728791
Exacrs794728791
Varsomers794728791
Maprs794728791
PheGenIrs794728791
hapmaprs794728791
1000 genomesrs794728791
hgdprs794728791
ensemblrs794728791
gopubmedrs794728791
geneviewrs794728791
scholarrs794728791
googlers794728791
pharmgkbrs794728791
gwascentralrs794728791
openSNPrs794728791
23andMers794728791
23andMe allrs794728791
SNP Nexus

SNPshotrs794728791
SNPdbers794728791
MSV3drs794728791
GWAS Ctlgrs794728791
Max Magnitude0
ClinVar
Risk rs794728791(A;A)
Alt rs794728791(A;A)
Reference rs794728791(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947595G>A
CLNSRC
CLNACC RCV000182825.1,