FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 731; N. variants: 141
Disease: Apert syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554927408
rs1554927408
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0001193
Disease:
Apert syndrome 		T 0.700 CausalMutation CLINVAR