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rs794728781

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728781(A;G)
Make rs794728781(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237783951
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728781
ebirs794728781
HLIrs794728781
Exacrs794728781
Varsomers794728781
Maprs794728781
PheGenIrs794728781
hapmaprs794728781
1000 genomesrs794728781
hgdprs794728781
ensemblrs794728781
gopubmedrs794728781
geneviewrs794728781
scholarrs794728781
googlers794728781
pharmgkbrs794728781
gwascentralrs794728781
openSNPrs794728781
23andMers794728781
23andMe allrs794728781
SNP Nexus

SNPshotrs794728781
SNPdbers794728781
MSV3drs794728781
GWAS Ctlgrs794728781
Max Magnitude0
ClinVar
Risk rs794728781(G;G)
Alt rs794728781(G;G)
Reference rs794728781(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947251A>G
CLNSRC
CLNACC RCV000182809.2,