{{Rsnum
|rsid=17458018
|Gene=FN1
|Chromosome=2
|position=215420652
|Orientation=plus
|GMAF=0.03352
|Gene_s=FN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 8.0 | 92.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 2.0 | 19.8 | 78.2
| LWK | 0.0 | 5.5 | 94.5
| MEX | 0.0 | 12.1 | 87.9
| MKK | 0.0 | 8.3 | 91.7
| TSI | 0.0 | 15.7 | 84.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22319020
|Trait=None
|Title=A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.
|RiskAllele=
|Pval=0.000007
|OR=1.2200
|ORtxt=None
|OA=1
}}

{{on chip | Illumina Human 1M}}