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rs794728748

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728748(A;A)
Make rs794728748(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237639026
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728748
ebirs794728748
HLIrs794728748
Exacrs794728748
Varsomers794728748
Maprs794728748
PheGenIrs794728748
hapmaprs794728748
1000 genomesrs794728748
hgdprs794728748
ensemblrs794728748
gopubmedrs794728748
geneviewrs794728748
scholarrs794728748
googlers794728748
pharmgkbrs794728748
gwascentralrs794728748
openSNPrs794728748
23andMers794728748
23andMe allrs794728748
SNP Nexus

SNPshotrs794728748
SNPdbers794728748
MSV3drs794728748
GWAS Ctlgrs794728748
Max Magnitude0
ClinVar
Risk rs794728748(A;A)
Alt rs794728748(A;A)
Reference rs794728748(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237802326G>A
CLNSRC
CLNACC RCV000182750.2,