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rs794728812

From SNPedia

Orientationplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs794728812(-;-)
Make rs794728812(-;AAG)
Make rs794728812(AAG;AAG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237377371
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728812
ebirs794728812
HLIrs794728812
Exacrs794728812
Varsomers794728812
Maprs794728812
PheGenIrs794728812
hapmaprs794728812
1000 genomesrs794728812
hgdprs794728812
ensemblrs794728812
gopubmedrs794728812
geneviewrs794728812
scholarrs794728812
googlers794728812
pharmgkbrs794728812
gwascentralrs794728812
openSNPrs794728812
23andMers794728812
23andMe allrs794728812
SNP Nexus

SNPshotrs794728812
SNPdbers794728812
MSV3drs794728812
GWAS Ctlgrs794728812
Max Magnitude0
ClinVar
Risk rs794728812(;)
Alt rs794728812(;)
Reference rs794728812(AGA;AGA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237540671_237540673delAAG
CLNSRC
CLNACC RCV000182856.1,