{{Rsnum
|rsid=2412488
|Gene=LNX1
|Chromosome=4
|position=53464700
|Orientation=plus
|GMAF=0.3301
|Gene_s=LNX1
|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 | 9.7 | 38.1 | 52.2
| HCB | 12.4 | 54.0 | 33.6
| JPT | 16.8 | 38.9 | 44.2
| YRI | 10.9 | 40.1 | 49.0
| ASW | 7.0 | 54.4 | 38.6
| CHB | 12.4 | 54.0 | 33.6
| CHD | 15.0 | 47.7 | 37.4
| GIH | 5.0 | 53.0 | 42.0
| LWK | 9.1 | 55.5 | 35.5
| MEX | 12.3 | 40.4 | 47.4
| MKK | 13.5 | 52.9 | 33.5
| TSI | 4.9 | 33.3 | 61.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23725790
  |Trait=DNA methylation (variation)
  |Title=GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
  |RiskAllele=A
  |Pval=9E-7
  |OR=NR
  |ORtxt=NR
  }}

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