{{Rsnum
|rsid=10930046
|Gene=IFIH1
|Chromosome=2
|position=162281473
|Orientation=plus
|GMAF=0.186
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=IFIH1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 2.7 | 97.3
| HCB | 2.2 | 21.3 | 76.5
| JPT | 0.9 | 19.6 | 79.5
| YRI | 32.0 | 47.6 | 20.4
| ASW | 12.3 | 54.4 | 33.3
| CHB | 2.2 | 21.3 | 76.5
| CHD | 0.9 | 21.1 | 78.0
| GIH | 0.0 | 3.0 | 97.0
| LWK | 20.9 | 49.1 | 30.0
| MEX | 5.4 | 42.9 | 51.8
| MKK | 1.9 | 30.1 | 67.9
| TSI | 0.0 | 2.0 | 98.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20668468
|Title=Carriers of rare missense variants in IFIH1 are protected from psoriasis
|OA=1
}}

{{PMID Auto
|PMID=19264985
|Title=Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes.
|OA=1
}}

{{GET Evidence
|gene=IFIH1
|aa_change=His460Arg
|aa_change_short=H460R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10930046
|overall_frequency_n=1641
|overall_frequency_d=10756
|overall_frequency=0.152566
|n_genomes=19
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23441136
|Title=Admixture Mapping in Lupus Identifies Multiple Functional Variants within IFIH1 Associated with Apoptosis, Inflammation, and Autoantibody Production
|OA=1
}}

{{PMID Auto
|PMID=23028602
|Title=Lactase persistence and lipid pathway selection in the Maasai.
|OA=1
}}

{{PMID Auto
|PMID=23246693
|Title=Interferon induced with helicase C domain 1 (IFIH1): trends on helicase domain and type 1 diabetes onset.
}}

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