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rs794728803

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728803(A;G)
Make rs794728803(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237806273
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728803
ebirs794728803
HLIrs794728803
Exacrs794728803
Varsomers794728803
Maprs794728803
PheGenIrs794728803
hapmaprs794728803
1000 genomesrs794728803
hgdprs794728803
ensemblrs794728803
gopubmedrs794728803
geneviewrs794728803
scholarrs794728803
googlers794728803
pharmgkbrs794728803
gwascentralrs794728803
openSNPrs794728803
23andMers794728803
23andMe allrs794728803
SNP Nexus

SNPshotrs794728803
SNPdbers794728803
MSV3drs794728803
GWAS Ctlgrs794728803
Max Magnitude0
ClinVar
Risk rs794728803(G;G)
Alt rs794728803(G;G)
Reference rs794728803(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237969573A>G
CLNSRC
CLNACC RCV000182844.1,