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rs398123072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123072(C;T)
Make rs398123072(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position75732682
GeneACADM
is asnp
is mentioned by
dbSNPrs398123072
ebirs398123072
HLIrs398123072
Exacrs398123072
Varsomers398123072
Maprs398123072
PheGenIrs398123072
hapmaprs398123072
1000 genomesrs398123072
hgdprs398123072
ensemblrs398123072
gopubmedrs398123072
geneviewrs398123072
scholarrs398123072
googlers398123072
pharmgkbrs398123072
gwascentralrs398123072
openSNPrs398123072
23andMers398123072
23andMe allrs398123072
SNP Nexus

SNPshotrs398123072
SNPdbers398123072
MSV3drs398123072
GWAS Ctlgrs398123072
Max Magnitude0
ClinVar
Risk rs398123072(T;T)
Alt rs398123072(T;T)
Reference rs398123072(C;C)
Significance Pathogenic
Disease not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76198367C>T
CLNSRC HGMD
CLNACC RCV000077882.3, RCV000176961.1,