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rs794728710

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728710(A;A)
Make rs794728710(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237388099
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728710
ebirs794728710
HLIrs794728710
Exacrs794728710
Varsomers794728710
Maprs794728710
PheGenIrs794728710
hapmaprs794728710
1000 genomesrs794728710
hgdprs794728710
ensemblrs794728710
gopubmedrs794728710
geneviewrs794728710
scholarrs794728710
googlers794728710
pharmgkbrs794728710
gwascentralrs794728710
openSNPrs794728710
23andMers794728710
23andMe allrs794728710
SNP Nexus

SNPshotrs794728710
SNPdbers794728710
MSV3drs794728710
GWAS Ctlgrs794728710
Max Magnitude0
ClinVar
Risk rs794728710(A;A)
Alt rs794728710(A;A)
Reference rs794728710(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237551399G>A
CLNSRC
CLNACC RCV000182662.2,