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rs398123073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123073(G;G)
Make rs398123073(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position75732743
GeneACADM
is asnp
is mentioned by
dbSNPrs398123073
ebirs398123073
HLIrs398123073
Exacrs398123073
Varsomers398123073
Maprs398123073
PheGenIrs398123073
hapmaprs398123073
1000 genomesrs398123073
hgdprs398123073
ensemblrs398123073
gopubmedrs398123073
geneviewrs398123073
scholarrs398123073
googlers398123073
pharmgkbrs398123073
gwascentralrs398123073
openSNPrs398123073
23andMers398123073
23andMe allrs398123073
SNP Nexus

SNPshotrs398123073
SNPdbers398123073
MSV3drs398123073
GWAS Ctlgrs398123073
Max Magnitude0
ClinVar
Risk rs398123073(G;G)
Alt rs398123073(G;G)
Reference rs398123073(T;T)
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.76198428T>G
CLNSRC ClinVar
CLNACC RCV000077884.3, RCV000176960.1,