{{Rsnum
|rsid=2039381
|Gene=IFNE
|Chromosome=9
|position=21481484
|Orientation=plus
|GMAF=0.06474
|Gene_s=IFNE,MIR31HG
|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 | 99.1 | 0.9 | 0.0
| HCB | 72.6 | 23.7 | 3.7
| JPT | 73.2 | 26.8 | 0.0
| YRI | 86.9 | 12.4 | 0.7
| ASW | 83.6 | 14.5 | 1.8
| CHB | 72.6 | 23.7 | 3.7
| CHD | 65.7 | 31.5 | 2.8
| GIH | 51.5 | 44.6 | 4.0
| LWK | 84.4 | 15.6 | 0.0
| MEX | 84.5 | 15.5 | 0.0
| MKK | 91.6 | 7.7 | 0.6
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=23802172
|Title=Association study between nonsense polymorphism (rs2039381, Gln71Stop) of Interferon-ε and susceptibility to vitiligo in Korean population
}}

{{PMID Auto
|PMID=24055696
|Title=T Allele of Nonsense Polymorphism (rs2039381, Gln71Stop) of Interferon-ε is a Risk Factor for the Development of Intracerebral Hemorrhage
}}

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