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rs794727694

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727694(C;C)
Make rs794727694(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75733527
GeneACADM
is asnp
is mentioned by
dbSNPrs794727694
ebirs794727694
HLIrs794727694
Exacrs794727694
Varsomers794727694
Maprs794727694
PheGenIrs794727694
hapmaprs794727694
1000 genomesrs794727694
hgdprs794727694
ensemblrs794727694
gopubmedrs794727694
geneviewrs794727694
scholarrs794727694
googlers794727694
pharmgkbrs794727694
gwascentralrs794727694
openSNPrs794727694
23andMers794727694
23andMe allrs794727694
SNP Nexus

SNPshotrs794727694
SNPdbers794727694
MSV3drs794727694
GWAS Ctlgrs794727694
Max Magnitude0
ClinVar
Risk rs794727694(C;C)
Alt rs794727694(C;C)
Reference rs794727694(G;G)
Significance Pathogenic
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76199212G>C
CLNSRC
CLNACC RCV000178700.1,