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rs794728809

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728809(C;C)
Make rs794728809(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237831561
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728809
ebirs794728809
HLIrs794728809
Exacrs794728809
Varsomers794728809
Maprs794728809
PheGenIrs794728809
hapmaprs794728809
1000 genomesrs794728809
hgdprs794728809
ensemblrs794728809
gopubmedrs794728809
geneviewrs794728809
scholarrs794728809
googlers794728809
pharmgkbrs794728809
gwascentralrs794728809
openSNPrs794728809
23andMers794728809
23andMe allrs794728809
SNP Nexus

SNPshotrs794728809
SNPdbers794728809
MSV3drs794728809
GWAS Ctlgrs794728809
Max Magnitude0
ClinVar
Risk rs794728809(C;C)
Alt rs794728809(C;C)
Reference rs794728809(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237994861G>C
CLNSRC
CLNACC RCV000182851.1,