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rs794728719

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728719(A;A)
Make rs794728719(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237441395
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728719
ebirs794728719
HLIrs794728719
Exacrs794728719
Varsomers794728719
Maprs794728719
PheGenIrs794728719
hapmaprs794728719
1000 genomesrs794728719
hgdprs794728719
ensemblrs794728719
gopubmedrs794728719
geneviewrs794728719
scholarrs794728719
googlers794728719
pharmgkbrs794728719
gwascentralrs794728719
openSNPrs794728719
23andMers794728719
23andMe allrs794728719
SNP Nexus

SNPshotrs794728719
SNPdbers794728719
MSV3drs794728719
GWAS Ctlgrs794728719
Max Magnitude0
ClinVar
Risk rs794728719(A;A)
Alt rs794728719(A;A)
Reference rs794728719(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene RYR2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.237604695G>A
CLNSRC
CLNACC RCV000223872.1,