Gene: FGFR2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2 		0.310 GeneticVariation disease LHGDN Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene. 16440883 2005
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2 		0.310 Biomarker disease GENOMICS_ENGLAND