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rs794728829

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728829(C;C)
Make rs794728829(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237791468
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728829
ebirs794728829
HLIrs794728829
Exacrs794728829
Varsomers794728829
Maprs794728829
PheGenIrs794728829
hapmaprs794728829
1000 genomesrs794728829
hgdprs794728829
ensemblrs794728829
gopubmedrs794728829
geneviewrs794728829
scholarrs794728829
googlers794728829
pharmgkbrs794728829
gwascentralrs794728829
openSNPrs794728829
23andMers794728829
23andMe allrs794728829
SNP Nexus

SNPshotrs794728829
SNPdbers794728829
MSV3drs794728829
GWAS Ctlgrs794728829
Max Magnitude0
ClinVar
Risk rs794728829(C;C)
Alt rs794728829(C;C)
Reference rs794728829(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237954768G>C
CLNSRC
CLNACC RCV000182892.1,