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

rs794728707

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728707(A;G)
Make rs794728707(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237377358
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728707
ebirs794728707
HLIrs794728707
Exacrs794728707
Varsomers794728707
Maprs794728707
PheGenIrs794728707
hapmaprs794728707
1000 genomesrs794728707
hgdprs794728707
ensemblrs794728707
gopubmedrs794728707
geneviewrs794728707
scholarrs794728707
googlers794728707
pharmgkbrs794728707
gwascentralrs794728707
openSNPrs794728707
23andMers794728707
23andMe allrs794728707
SNP Nexus

SNPshotrs794728707
SNPdbers794728707
MSV3drs794728707
GWAS Ctlgrs794728707
Max Magnitude0
ClinVar
Risk rs794728707(G;G)
Alt rs794728707(G;G)
Reference rs794728707(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237540658A>G
CLNSRC
CLNACC RCV000182657.1,