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rs794728787

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728787(A;G)
Make rs794728787(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784245
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728787
ebirs794728787
HLIrs794728787
Exacrs794728787
Varsomers794728787
Maprs794728787
PheGenIrs794728787
hapmaprs794728787
1000 genomesrs794728787
hgdprs794728787
ensemblrs794728787
gopubmedrs794728787
geneviewrs794728787
scholarrs794728787
googlers794728787
pharmgkbrs794728787
gwascentralrs794728787
openSNPrs794728787
23andMers794728787
23andMe allrs794728787
SNP Nexus

SNPshotrs794728787
SNPdbers794728787
MSV3drs794728787
GWAS Ctlgrs794728787
Max Magnitude0
ClinVar
Risk rs794728787(G;G)
Alt rs794728787(G;G)
Reference rs794728787(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947545A>G
CLNSRC
CLNACC RCV000182820.1,