FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 731; N. variants: 141
Disease: Congenital Microtia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3850155
Disease: Congenital Microtia
Congenital Microtia 		0.010 GeneticVariation disease BEFREE The rs3135718-G gene in FGFR2 has a certain association with the incidence of congenital microtia with high prevalence and risk. 31258676 2019