View source for Rs12205363

{{Rsnum
|rsid=12205363
|Gene=LAMA2
|Chromosome=6
|position=129513484
|Orientation=plus
|GMAF=0.03673
|Gene_s=LAMA2,LOC102723409
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|StabilizedOrientation=plus
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 15.9 | 83.2
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 1.4 | 98.6
| ASW | 1.8 | 0.0 | 98.2
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 4.0 | 96.0
| LWK | 0.0 | 4.6 | 95.4
| MEX | 0.0 | 1.7 | 98.3
| MKK | 0.0 | 11.7 | 88.3
| TSI | 0.0 | 8.8 | 91.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23396134
  |Trait=Refractive error
  |Title=Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
  |RiskAllele=C
  |Pval=2E-12
  |OR=.24
  |ORtxt=[0.17-0.3] unit increase
  |OA=1
}}

Occurs within the LAMA2 (Laminin alpha-2) gene

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Ancestry v2}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | 23andMe v5}}
{{on chip | Ancestry v2c}}
{{on chip | Ancestry v2d}}