Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728804

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728804(A;A)
Make rs794728804(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237808913
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728804
ebirs794728804
HLIrs794728804
Exacrs794728804
Varsomers794728804
Maprs794728804
PheGenIrs794728804
hapmaprs794728804
1000 genomesrs794728804
hgdprs794728804
ensemblrs794728804
gopubmedrs794728804
geneviewrs794728804
scholarrs794728804
googlers794728804
pharmgkbrs794728804
gwascentralrs794728804
openSNPrs794728804
23andMers794728804
23andMe allrs794728804
SNP Nexus

SNPshotrs794728804
SNPdbers794728804
MSV3drs794728804
GWAS Ctlgrs794728804
Max Magnitude0
ClinVar
Risk rs794728804(A;A)
Alt rs794728804(A;A)
Reference rs794728804(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237972213G>A
CLNSRC
CLNACC RCV000182845.1,