{{Rsnum
|rsid=13317
|Gene=FGFR1
|Chromosome=8
|position=38411996
|Orientation=plus
|GMAF=0.2759
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FGFR1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 7.1 | 41.6 | 51.3
| HCB | 12.4 | 48.2 | 39.4
| JPT | 15.9 | 46.0 | 38.1
| YRI | 1.4 | 30.6 | 68.0
| ASW | 5.3 | 33.3 | 61.4
| CHB | 12.4 | 48.2 | 39.4
| CHD | 14.7 | 43.1 | 42.2
| GIH | 1.0 | 16.8 | 82.2
| LWK | 10.9 | 30.0 | 59.1
| MEX | 6.9 | 46.6 | 46.6
| MKK | 8.3 | 47.4 | 44.2
| TSI | 6.9 | 37.3 | 55.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=19727229
|Title=Correlation of the SNPs of FGFR1, FGF10, FGF18 with nonsyndromic cleft lip with or without palate in Chinese population
}}

{{PMID|17318851|OA=1
}} Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.

{{PMID|17360555|OA=1
}} Impaired FGF signaling contributes to cleft lip and palate.

{{PMID|17366557|OA=1
}} A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23.

{{PMID|18478591|OA=1
}} Studies of genes in the FGF signaling pathway and oral clefts with or without dental anomalies.

{{PMID Auto
|PMID=23939983
|Title=Polymorphisms in BMP4 and FGFR1 genes are associated with fracture non-union
}}

{{PMID Auto
|PMID=24129055
|Title=Evidence of genetic variations associated with rotator cuff disease
}}

{{PMID Auto
|PMID=24385678
|Title=Involvement of fibroblast growth factor receptor genes in benign prostate hyperplasia in a Korean population
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}