EPHB1, EPH receptor B1, 2047

N. diseases: 169; N. variants: 17
Disease: Total iron binding capacity function ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935 2017