{{Rsnum
|rsid=13422767
|Gene=FAP
|Chromosome=2
|position=162243749
|Orientation=plus
|GMAF=0.1483
|Gene_s=FAP
|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 | 1.8 | 24.8 | 73.5
| HCB | 9.5 | 43.8 | 46.7
| JPT | 3.6 | 36.6 | 59.8
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.4 | 94.6
| CHB | 9.5 | 43.8 | 46.7
| CHD | 13.0 | 38.9 | 48.1
| GIH | 21.8 | 41.6 | 36.6
| LWK | 0.0 | 0.0 | 0.0
| MEX | 3.4 | 19.0 | 77.6
| MKK | 0.0 | 3.2 | 96.8
| TSI | 2.0 | 35.3 | 62.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22789000
|Title=Polymorphisms in the interferon-induced helicase (IFIH1) locus and susceptibility to Addison's disease
}}

{{PMID Auto
|PMID=18285833
|Title=IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk.
}}

{{PMID Auto
|PMID=18927125
|Title=IFIH1 polymorphisms are significantly associated with type 1 diabetes and IFIH1 gene expression in peripheral blood mononuclear cells.
|OA=1
}}

{{PMID Auto
|PMID=19956109
|Title=The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.
|OA=1
}}

{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}