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rs794728784

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728784(A;G)
Make rs794728784(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784002
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728784
ebirs794728784
HLIrs794728784
Exacrs794728784
Varsomers794728784
Maprs794728784
PheGenIrs794728784
hapmaprs794728784
1000 genomesrs794728784
hgdprs794728784
ensemblrs794728784
gopubmedrs794728784
geneviewrs794728784
scholarrs794728784
googlers794728784
pharmgkbrs794728784
gwascentralrs794728784
openSNPrs794728784
23andMers794728784
23andMe allrs794728784
SNP Nexus

SNPshotrs794728784
SNPdbers794728784
MSV3drs794728784
GWAS Ctlgrs794728784
Max Magnitude0
ClinVar
Risk rs794728784(G;G)
Alt rs794728784(G;G)
Reference rs794728784(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947302A>G
CLNSRC
CLNACC RCV000182813.1,