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rs794728740

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728740(A;A)
Make rs794728740(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237614298
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728740
ebirs794728740
HLIrs794728740
Exacrs794728740
Varsomers794728740
Maprs794728740
PheGenIrs794728740
hapmaprs794728740
1000 genomesrs794728740
hgdprs794728740
ensemblrs794728740
gopubmedrs794728740
geneviewrs794728740
scholarrs794728740
googlers794728740
pharmgkbrs794728740
gwascentralrs794728740
openSNPrs794728740
23andMers794728740
23andMe allrs794728740
SNP Nexus

SNPshotrs794728740
SNPdbers794728740
MSV3drs794728740
GWAS Ctlgrs794728740
Max Magnitude0
ClinVar
Risk rs794728740(A;A)
Alt rs794728740(A;A)
Reference rs794728740(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237777598G>A
CLNSRC
CLNACC RCV000182731.2,