Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728713

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728713(C;C)
Make rs794728713(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237417065
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728713
ebirs794728713
HLIrs794728713
Exacrs794728713
Varsomers794728713
Maprs794728713
PheGenIrs794728713
hapmaprs794728713
1000 genomesrs794728713
hgdprs794728713
ensemblrs794728713
gopubmedrs794728713
geneviewrs794728713
scholarrs794728713
googlers794728713
pharmgkbrs794728713
gwascentralrs794728713
openSNPrs794728713
23andMers794728713
23andMe allrs794728713
SNP Nexus

SNPshotrs794728713
SNPdbers794728713
MSV3drs794728713
GWAS Ctlgrs794728713
Max Magnitude0
ClinVar
Risk rs794728713(C;C)
Alt rs794728713(C;C)
Reference rs794728713(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237580365G>C
CLNSRC
CLNACC RCV000182666.2,