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rs794728788

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728788(A;C)
Make rs794728788(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784257
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728788
ebirs794728788
HLIrs794728788
Exacrs794728788
Varsomers794728788
Maprs794728788
PheGenIrs794728788
hapmaprs794728788
1000 genomesrs794728788
hgdprs794728788
ensemblrs794728788
gopubmedrs794728788
geneviewrs794728788
scholarrs794728788
googlers794728788
pharmgkbrs794728788
gwascentralrs794728788
openSNPrs794728788
23andMers794728788
23andMe allrs794728788
SNP Nexus

SNPshotrs794728788
SNPdbers794728788
MSV3drs794728788
GWAS Ctlgrs794728788
Max Magnitude0
ClinVar
Risk rs794728788(C;C)
Alt rs794728788(C;C)
Reference rs794728788(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947557A>C
CLNSRC
CLNACC RCV000182822.1,