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rs794728814

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728814(A;G)
Make rs794728814(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237377427
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728814
ebirs794728814
HLIrs794728814
Exacrs794728814
Varsomers794728814
Maprs794728814
PheGenIrs794728814
hapmaprs794728814
1000 genomesrs794728814
hgdprs794728814
ensemblrs794728814
gopubmedrs794728814
geneviewrs794728814
scholarrs794728814
googlers794728814
pharmgkbrs794728814
gwascentralrs794728814
openSNPrs794728814
23andMers794728814
23andMe allrs794728814
SNP Nexus

SNPshotrs794728814
SNPdbers794728814
MSV3drs794728814
GWAS Ctlgrs794728814
Max Magnitude0
ClinVar
Risk rs794728814(G;G)
Alt rs794728814(G;G)
Reference rs794728814(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237540727A>G
CLNSRC
CLNACC RCV000182858.2,