EPO, erythropoietin, 2056

N. diseases: 646; N. variants: 11
Disease: Retinopathy of Prematurity ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1617640
rs1617640
Entrez Id: 2056
Gene Symbol: EPO
EPO
CUI: C0035344
Disease:
Retinopathy of Prematurity 		0.010 GeneticVariation BEFREE The Erythropoietin Promoter Variant rs1617640 Is Not Associated with Severe Retinopathy of Prematurity, Independent of Treatment with Erythropoietin. 29731355 2018