{{Rsnum
|rsid=152528
|Gene=FGF1
|Chromosome=5
|position=142638295
|Orientation=plus
|GMAF=0.2475
|Gene_s=FGF1
|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 | 18.6 | 38.9 | 42.5
| HCB | 6.6 | 33.6 | 59.9
| JPT | 5.3 | 33.6 | 61.1
| YRI | 0.0 | 6.8 | 93.2
| ASW | 8.8 | 17.5 | 73.7
| CHB | 6.6 | 33.6 | 59.9
| CHD | 3.7 | 38.9 | 57.4
| GIH | 12.9 | 40.6 | 46.5
| LWK | 0.0 | 7.3 | 92.7
| MEX | 5.2 | 36.2 | 58.6
| MKK | 2.6 | 23.7 | 73.7
| TSI | 16.8 | 51.5 | 31.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21348951
|Trait=None
|Title=Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality
|RiskAllele=
|Pval=8E-7
|OR=None
|ORtxt=None
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}