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rs794728801

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728801(C;C)
Make rs794728801(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237806144
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728801
ebirs794728801
HLIrs794728801
Exacrs794728801
Varsomers794728801
Maprs794728801
PheGenIrs794728801
hapmaprs794728801
1000 genomesrs794728801
hgdprs794728801
ensemblrs794728801
gopubmedrs794728801
geneviewrs794728801
scholarrs794728801
googlers794728801
pharmgkbrs794728801
gwascentralrs794728801
openSNPrs794728801
23andMers794728801
23andMe allrs794728801
SNP Nexus

SNPshotrs794728801
SNPdbers794728801
MSV3drs794728801
GWAS Ctlgrs794728801
Max Magnitude0
ClinVar
Risk rs794728801(C;C)
Alt rs794728801(C;C)
Reference rs794728801(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237969444T>C
CLNSRC
CLNACC RCV000182842.1,