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rs794728813

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728813(C;T)
Make rs794728813(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237330893
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728813
ebirs794728813
HLIrs794728813
Exacrs794728813
Varsomers794728813
Maprs794728813
PheGenIrs794728813
hapmaprs794728813
1000 genomesrs794728813
hgdprs794728813
ensemblrs794728813
gopubmedrs794728813
geneviewrs794728813
scholarrs794728813
googlers794728813
pharmgkbrs794728813
gwascentralrs794728813
openSNPrs794728813
23andMers794728813
23andMe allrs794728813
SNP Nexus

SNPshotrs794728813
SNPdbers794728813
MSV3drs794728813
GWAS Ctlgrs794728813
Max Magnitude0
ClinVar
Risk rs794728813(T;T)
Alt rs794728813(T;T)
Reference rs794728813(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237494193C>T
CLNSRC
CLNACC RCV000182857.1,