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rs794728826

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728826(A;A)
Make rs794728826(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237781618
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728826
ebirs794728826
HLIrs794728826
Exacrs794728826
Varsomers794728826
Maprs794728826
PheGenIrs794728826
hapmaprs794728826
1000 genomesrs794728826
hgdprs794728826
ensemblrs794728826
gopubmedrs794728826
geneviewrs794728826
scholarrs794728826
googlers794728826
pharmgkbrs794728826
gwascentralrs794728826
openSNPrs794728826
23andMers794728826
23andMe allrs794728826
SNP Nexus

SNPshotrs794728826
SNPdbers794728826
MSV3drs794728826
GWAS Ctlgrs794728826
Max Magnitude0
ClinVar
Risk rs794728826(A;A)
Alt rs794728826(A;A)
Reference rs794728826(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237944918G>A
CLNSRC
CLNACC RCV000182888.1,