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rs794728790

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728790(A;A)
Make rs794728790(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784271
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728790
ebirs794728790
HLIrs794728790
Exacrs794728790
Varsomers794728790
Maprs794728790
PheGenIrs794728790
hapmaprs794728790
1000 genomesrs794728790
hgdprs794728790
ensemblrs794728790
gopubmedrs794728790
geneviewrs794728790
scholarrs794728790
googlers794728790
pharmgkbrs794728790
gwascentralrs794728790
openSNPrs794728790
23andMers794728790
23andMe allrs794728790
SNP Nexus

SNPshotrs794728790
SNPdbers794728790
MSV3drs794728790
GWAS Ctlgrs794728790
Max Magnitude0
ClinVar
Risk rs794728790(A;A)
Alt rs794728790(A;A)
Reference rs794728790(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947571G>A
CLNSRC
CLNACC RCV000182824.1,