{{Rsnum
|rsid=6430585
|Gene=UBXN4
|Chromosome=2
|position=135749357
|Orientation=plus
|GMAF=0.2911
|Gene_s=UBXN4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 3.5 | 21.2 | 75.2
| HCB | 5.1 | 34.3 | 60.6
| JPT | 2.7 | 33.6 | 63.7
| YRI | 15.0 | 42.2 | 42.9
| ASW | 15.8 | 40.4 | 43.9
| CHB | 5.1 | 34.3 | 60.6
| CHD | 3.7 | 37.6 | 58.7
| GIH | 10.9 | 44.6 | 44.6
| LWK | 20.9 | 41.8 | 37.3
| MEX | 8.6 | 37.9 | 53.4
| MKK | 71.6 | 27.1 | 1.3
| TSI | 24.5 | 47.1 | 28.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21979947
|Trait=None
|Title=A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.
|RiskAllele=
|Pval=0.000001
|OR=1.3900
|ORtxt=[NR]
|OA=1
}}

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