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rs794728705

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728705(G;G)
Make rs794728705(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237330927
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728705
ebirs794728705
HLIrs794728705
Exacrs794728705
Varsomers794728705
Maprs794728705
PheGenIrs794728705
hapmaprs794728705
1000 genomesrs794728705
hgdprs794728705
ensemblrs794728705
gopubmedrs794728705
geneviewrs794728705
scholarrs794728705
googlers794728705
pharmgkbrs794728705
gwascentralrs794728705
openSNPrs794728705
23andMers794728705
23andMe allrs794728705
SNP Nexus

SNPshotrs794728705
SNPdbers794728705
MSV3drs794728705
GWAS Ctlgrs794728705
Max Magnitude0
ClinVar
Risk rs794728705(G;G)
Alt rs794728705(G;G)
Reference rs794728705(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237494227T>G
CLNSRC
CLNACC RCV000182652.1,