{{Rsnum
|rsid=930847
|Gene=LRRK1
|Chromosome=15
|position=101018357
|Orientation=minus
|GMAF=0.2883
|Gene_s=LRRK1
|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 | 61.9 | 36.3 | 1.8
| HCB | 67.2 | 27.7 | 5.1
| JPT | 62.8 | 32.7 | 4.4
| YRI | 10.9 | 37.4 | 51.7
| ASW | 28.6 | 28.6 | 42.9
| CHB | 67.2 | 27.7 | 5.1
| CHD | 62.4 | 36.7 | 0.9
| GIH | 69.0 | 26.0 | 5.0
| LWK | 22.0 | 48.6 | 29.4
| MEX | 70.7 | 25.9 | 3.4
| MKK | 40.0 | 49.0 | 11.0
| TSI | 53.9 | 37.3 | 8.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23291589
  |Trait=Corneal structure
  |Title=Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
  |RiskAllele=T
  |Pval=6E-19
  |OR=.11
  |ORtxt=[0.071-0.149] unit decrease
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}