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rs794728744

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728744(G;T)
Make rs794728744(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237633705
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728744
ebirs794728744
HLIrs794728744
Exacrs794728744
Varsomers794728744
Maprs794728744
PheGenIrs794728744
hapmaprs794728744
1000 genomesrs794728744
hgdprs794728744
ensemblrs794728744
gopubmedrs794728744
geneviewrs794728744
scholarrs794728744
googlers794728744
pharmgkbrs794728744
gwascentralrs794728744
openSNPrs794728744
23andMers794728744
23andMe allrs794728744
SNP Nexus

SNPshotrs794728744
SNPdbers794728744
MSV3drs794728744
GWAS Ctlgrs794728744
Max Magnitude0
ClinVar
Risk rs794728744(T;T)
Alt rs794728744(T;T)
Reference rs794728744(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237797005G>T
CLNSRC
CLNACC RCV000182745.2,