{{Rsnum
|rsid=11260867
|Gene=EPHA2
|Chromosome=1
|position=16115233
|Orientation=plus
|GMAF=0.08861
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 62.5 | 37.5 | 0.0
| HCB | 97.8 | 2.2 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 95.2 | 4.8 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 97.8 | 2.2 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}[[rs11260867]] is a SNP located 3' of the [[EPHA2]] gene, which has at least one putative causative mutation leading to age-related [[cataracts]]. {{PMID|19005574|OA=1
}}

A study involving a case-control cohort from Northern Italy, comprising 126 unrelated individuals with nuclear cataracts, 119 with cortical cataracts, and 104 unrelated controls with clear lenses, found increased risk associated two SNPs near the [[EPHA2]] gene ([[rs7543472]] and [[rs11260867]]). For [[rs11260867]], the (G;G) genotype was as 1.5 - 2.3x increased risk for [[cataracts]] (p < 0.007). {{PMID|19005574|OA=1
}}

{{omim
|id=116600
|rsnum=11260867
}}

{{omim
|id=613020
|rsnum=11260867
}}

{{on chip | Affy GenomeWide 6}}