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rs794728806

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728806(C;C)
Make rs794728806(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237828413
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728806
ebirs794728806
HLIrs794728806
Exacrs794728806
Varsomers794728806
Maprs794728806
PheGenIrs794728806
hapmaprs794728806
1000 genomesrs794728806
hgdprs794728806
ensemblrs794728806
gopubmedrs794728806
geneviewrs794728806
scholarrs794728806
googlers794728806
pharmgkbrs794728806
gwascentralrs794728806
openSNPrs794728806
23andMers794728806
23andMe allrs794728806
SNP Nexus

SNPshotrs794728806
SNPdbers794728806
MSV3drs794728806
GWAS Ctlgrs794728806
Max Magnitude0
ClinVar
Risk rs794728806(C;C)
Alt rs794728806(C;C)
Reference rs794728806(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237991713G>C
CLNSRC
CLNACC RCV000182848.1,