{{Rsnum
|rsid=4954218
|Chromosome=2
|position=135045855
|Orientation=plus
|GMAF=0.0978
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 8.0 | 40.7 | 51.3
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 1.8 | 10.5 | 87.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 26.7 | 72.3
| LWK | 0.0 | 0.0 | 0.0
| MEX | 1.7 | 29.3 | 69.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 10.8 | 89.2
| 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=1E-9
|OR=1.6100
|ORtxt=[NR]
|OA=1
}}

{{PMID Auto
|PMID=23833071
|Title=Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconus
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}