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rs794728751

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728751(A;A)
Make rs794728751(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237639111
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728751
ebirs794728751
HLIrs794728751
Exacrs794728751
Varsomers794728751
Maprs794728751
PheGenIrs794728751
hapmaprs794728751
1000 genomesrs794728751
hgdprs794728751
ensemblrs794728751
gopubmedrs794728751
geneviewrs794728751
scholarrs794728751
googlers794728751
pharmgkbrs794728751
gwascentralrs794728751
openSNPrs794728751
23andMers794728751
23andMe allrs794728751
SNP Nexus

SNPshotrs794728751
SNPdbers794728751
MSV3drs794728751
GWAS Ctlgrs794728751
Max Magnitude0
ClinVar
Risk rs794728751(A;A)
Alt rs794728751(A;A)
Reference rs794728751(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237802411G>A
CLNSRC
CLNACC RCV000182753.1,