DECR1, 2,4-dienoyl-CoA reductase 1, 1666

N. diseases: 399; N. variants: 8
Disease: Congenital Abnormality ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201405525
rs201405525
Entrez Id: 1666
Gene Symbol: DECR1
DECR1
CUI: C0000768
Disease:
Congenital Abnormality 		0.010 GeneticVariation BEFREE The human POR mutation A287P presents with disordered sexual development and skeletal malformations. 27496950 2016