FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 731; N. variants: 141
Disease: Congenital Microtia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3135718
rs3135718
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C3850155
Disease:
Congenital Microtia 		0.010 GeneticVariation BEFREE The rs3135718-G gene in FGFR2 has a certain association with the incidence of congenital microtia with high prevalence and risk. 31258676 2019