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rs794728718

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728718(G;G)
Make rs794728718(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237441379
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728718
ebirs794728718
HLIrs794728718
Exacrs794728718
Varsomers794728718
Maprs794728718
PheGenIrs794728718
hapmaprs794728718
1000 genomesrs794728718
hgdprs794728718
ensemblrs794728718
gopubmedrs794728718
geneviewrs794728718
scholarrs794728718
googlers794728718
pharmgkbrs794728718
gwascentralrs794728718
openSNPrs794728718
23andMers794728718
23andMe allrs794728718
SNP Nexus

SNPshotrs794728718
SNPdbers794728718
MSV3drs794728718
GWAS Ctlgrs794728718
Max Magnitude0
ClinVar
Risk rs794728718(G;G)
Alt rs794728718(G;G)
Reference rs794728718(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237604679T>G
CLNSRC
CLNACC RCV000182672.1,