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rs794728715

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728715(C;T)
Make rs794728715(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237417093
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728715
ebirs794728715
HLIrs794728715
Exacrs794728715
Varsomers794728715
Maprs794728715
PheGenIrs794728715
hapmaprs794728715
1000 genomesrs794728715
hgdprs794728715
ensemblrs794728715
gopubmedrs794728715
geneviewrs794728715
scholarrs794728715
googlers794728715
pharmgkbrs794728715
gwascentralrs794728715
openSNPrs794728715
23andMers794728715
23andMe allrs794728715
SNP Nexus

SNPshotrs794728715
SNPdbers794728715
MSV3drs794728715
GWAS Ctlgrs794728715
Max Magnitude0
ClinVar
Risk rs794728715(T;T)
Alt rs794728715(T;T)
Reference rs794728715(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237580393C>T
CLNSRC
CLNACC RCV000182668.1,