{{Rsnum
|rsid=975121
|Gene=FGF12
|Chromosome=3
|position=192179429
|Orientation=plus
|GMAF=0.2658
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FGF12
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.4 | 45.1 | 27.4
| HCB | 87.5 | 12.5 | 0.0
| JPT | 87.6 | 12.4 | 0.0
| YRI | 95.9 | 4.1 | 0.0
| ASW | 82.5 | 17.5 | 0.0
| CHB | 87.5 | 12.5 | 0.0
| CHD | 90.7 | 9.3 | 0.0
| GIH | 51.5 | 43.6 | 5.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 41.4 | 50.0 | 8.6
| MKK | 80.6 | 18.1 | 1.3
| TSI | 16.0 | 61.0 | 23.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21139019
|Trait=None
|Title=A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum
|RiskAllele=
|Pval=0.000007
|OR=2.1700
|ORtxt=[1.55-3.03]
|OA=1
}}

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