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rs794728745

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728745(A;A)
Make rs794728745(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237638447
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728745
ebirs794728745
HLIrs794728745
Exacrs794728745
Varsomers794728745
Maprs794728745
PheGenIrs794728745
hapmaprs794728745
1000 genomesrs794728745
hgdprs794728745
ensemblrs794728745
gopubmedrs794728745
geneviewrs794728745
scholarrs794728745
googlers794728745
pharmgkbrs794728745
gwascentralrs794728745
openSNPrs794728745
23andMers794728745
23andMe allrs794728745
SNP Nexus

SNPshotrs794728745
SNPdbers794728745
MSV3drs794728745
GWAS Ctlgrs794728745
Max Magnitude0
ClinVar
Risk rs794728745(A;A)
Alt rs794728745(A;A)
Reference rs794728745(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237801747G>A
CLNSRC
CLNACC RCV000182747.1,