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rs794728758

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728758(A;G)
Make rs794728758(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237654304
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728758
ebirs794728758
HLIrs794728758
Exacrs794728758
Varsomers794728758
Maprs794728758
PheGenIrs794728758
hapmaprs794728758
1000 genomesrs794728758
hgdprs794728758
ensemblrs794728758
gopubmedrs794728758
geneviewrs794728758
scholarrs794728758
googlers794728758
pharmgkbrs794728758
gwascentralrs794728758
openSNPrs794728758
23andMers794728758
23andMe allrs794728758
SNP Nexus

SNPshotrs794728758
SNPdbers794728758
MSV3drs794728758
GWAS Ctlgrs794728758
Max Magnitude0
ClinVar
Risk rs794728758(G;G)
Alt rs794728758(G;G)
Reference rs794728758(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237817604A>G
CLNSRC
CLNACC RCV000182763.2,