{{Rsnum
|rsid=12193446
|Gene=LAMA2
|Chromosome=6
|position=129498893
|Orientation=plus
|GMAF=0.03949
|Gene_s=LAMA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 78.8 | 20.4 | 0.9
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 96.5 | 1.8 | 1.8
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 93.1 | 6.9 | 0.0
| LWK | 97.3 | 2.7 | 0.0
| MEX | 98.3 | 1.7 | 0.0
| MKK | 93.6 | 6.4 | 0.0
| TSI | 87.3 | 11.8 | 1.0
| HapMapRevision=28
}}risk of nearsightedness in people with European ancestry 
http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1003299

{{PMID Auto GWAS
  |PMID=24144296
  |Trait=Axial length
  |Title=Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.
  |RiskAllele=A
  |Pval=1E-8
  |OR=.12
  |ORtxt=[0.08-0.164] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}