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rs794728757

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728757(C;T)
Make rs794728757(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237648486
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728757
ebirs794728757
HLIrs794728757
Exacrs794728757
Varsomers794728757
Maprs794728757
PheGenIrs794728757
hapmaprs794728757
1000 genomesrs794728757
hgdprs794728757
ensemblrs794728757
gopubmedrs794728757
geneviewrs794728757
scholarrs794728757
googlers794728757
pharmgkbrs794728757
gwascentralrs794728757
openSNPrs794728757
23andMers794728757
23andMe allrs794728757
SNP Nexus

SNPshotrs794728757
SNPdbers794728757
MSV3drs794728757
GWAS Ctlgrs794728757
Max Magnitude0
ClinVar
Risk rs794728757(T;T)
Alt rs794728757(T;T)
Reference rs794728757(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237811786C>T
CLNSRC
CLNACC RCV000182762.1,