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

N. diseases: 399; N. variants: 8
Disease: Hemophagocytic Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs752317734
rs752317734
Entrez Id: 1666
Gene Symbol: DECR1
DECR1
CUI: C3887558
Disease:
Hemophagocytic Syndrome 		0.010 GeneticVariation BEFREE Recurrent ECSIT mutation encoding V140A triggers hyperinflammation and promotes hemophagocytic syndrome in extranodal NK/T cell lymphoma. 29291352 2018