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rs794728711

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728711(A;A)
Make rs794728711(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237388114
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728711
ebirs794728711
HLIrs794728711
Exacrs794728711
Varsomers794728711
Maprs794728711
PheGenIrs794728711
hapmaprs794728711
1000 genomesrs794728711
hgdprs794728711
ensemblrs794728711
gopubmedrs794728711
geneviewrs794728711
scholarrs794728711
googlers794728711
pharmgkbrs794728711
gwascentralrs794728711
openSNPrs794728711
23andMers794728711
23andMe allrs794728711
SNP Nexus

SNPshotrs794728711
SNPdbers794728711
MSV3drs794728711
GWAS Ctlgrs794728711
Max Magnitude0
ClinVar
Risk rs794728711(A;A)
Alt rs794728711(A;A)
Reference rs794728711(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237551414G>A
CLNSRC
CLNACC RCV000182663.2,