{{Rsnum
|rsid=1250248
|Gene=FN1
|Chromosome=2
|position=215422370
|Orientation=plus
|GMAF=0.1607
|Gene_s=FN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.6 | 33.9 | 62.5
| HCB | 0.0 | 12.4 | 87.6
| JPT | 0.9 | 3.6 | 95.5
| YRI | 0.0 | 29.0 | 71.0
| ASW | 8.8 | 29.8 | 61.4
| CHB | 0.0 | 12.4 | 87.6
| CHD | 0.9 | 21.1 | 78.0
| GIH | 15.8 | 53.5 | 30.7
| LWK | 1.8 | 34.5 | 63.6
| MEX | 1.7 | 32.8 | 65.5
| MKK | 5.2 | 32.9 | 61.9
| TSI | 5.9 | 40.2 | 53.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=23142796
|Title=An Italian association study and meta-analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first identified susceptibility loci for endometriosis
}}

{{PMID Auto
|PMID=23315067
|Title=Replication of endometriosis-associated single-nucleotide polymorphisms from genome-wide association studies in a Caucasian population.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}