{{Rsnum
|rsid=3779748
|Gene=EYA1
|Chromosome=8
|position=71335939
|Orientation=plus
|GMAF=0.4509
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=EYA1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 13.3 | 39.8 | 46.9
| HCB | 54.7 | 39.4 | 5.8
| JPT | 49.6 | 46.0 | 4.4
| YRI | 2.0 | 48.3 | 49.7
| ASW | 10.5 | 36.8 | 52.6
| CHB | 54.7 | 39.4 | 5.8
| CHD | 56.9 | 37.6 | 5.5
| GIH | 12.9 | 56.4 | 30.7
| LWK | 14.5 | 40.9 | 44.5
| MEX | 41.4 | 32.8 | 25.9
| MKK | 9.0 | 42.3 | 48.7
| TSI | 9.8 | 33.3 | 56.9
| HapMapRevision=28
}}

{{PMID|18522750|OA=1
}} [[rs3779748]] in EYA1, was significantly associated with [[kidney disease]] (odds ratio per each T allele 1.22, p=0.01)

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}