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rs794728789

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728789(A;G)
Make rs794728789(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784263
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728789
ebirs794728789
HLIrs794728789
Exacrs794728789
Varsomers794728789
Maprs794728789
PheGenIrs794728789
hapmaprs794728789
1000 genomesrs794728789
hgdprs794728789
ensemblrs794728789
gopubmedrs794728789
geneviewrs794728789
scholarrs794728789
googlers794728789
pharmgkbrs794728789
gwascentralrs794728789
openSNPrs794728789
23andMers794728789
23andMe allrs794728789
SNP Nexus

SNPshotrs794728789
SNPdbers794728789
MSV3drs794728789
GWAS Ctlgrs794728789
Max Magnitude0
ClinVar
Risk rs794728789(G;G)
Alt rs794728789(G;G)
Reference rs794728789(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947563A>G
CLNSRC
CLNACC RCV000182823.1,