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rs794728786

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728786(A;A)
Make rs794728786(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784182
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728786
ebirs794728786
HLIrs794728786
Exacrs794728786
Varsomers794728786
Maprs794728786
PheGenIrs794728786
hapmaprs794728786
1000 genomesrs794728786
hgdprs794728786
ensemblrs794728786
gopubmedrs794728786
geneviewrs794728786
scholarrs794728786
googlers794728786
pharmgkbrs794728786
gwascentralrs794728786
openSNPrs794728786
23andMers794728786
23andMe allrs794728786
SNP Nexus

SNPshotrs794728786
SNPdbers794728786
MSV3drs794728786
GWAS Ctlgrs794728786
Max Magnitude0
ClinVar
Risk rs794728786(A;A)
Alt rs794728786(A;A)
Reference rs794728786(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947482G>A
CLNSRC
CLNACC RCV000182819.2,