FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 731; N. variants: 141
Disease: Malocclusion ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10736303
rs10736303
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0024636
Disease:
Malocclusion 		0.010 GeneticVariation BEFREE Five SNPs (rs2162540, rs2981578, rs1078806, rs11200014, and rs10736303) were found to be associated with skeletal malocclusions (all <i>P</i> < 0.05). 31509720 2019