{{Rsnum
|rsid=6941712
|Gene=EPB41L2
|Chromosome=6
|position=130961070
|Orientation=plus
|GMAF=0.2782
|Gene_s=EPB41L2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 6.2 | 22.1 | 71.7
| HCB | 21.3 | 48.5 | 30.1
| JPT | 31.9 | 40.7 | 27.4
| YRI | 14.4 | 36.3 | 49.3
| ASW | 10.5 | 29.8 | 59.6
| CHB | 21.3 | 48.5 | 30.1
| CHD | 13.9 | 55.6 | 30.6
| GIH | 1.0 | 28.7 | 70.3
| LWK | 10.3 | 42.1 | 47.7
| MEX | 12.1 | 37.9 | 50.0
| MKK | 4.5 | 42.3 | 53.2
| TSI | 2.9 | 28.4 | 68.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22903471
  |Trait=Lentiform nucleus volume
  |Title=Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.
  |RiskAllele=C
  |Pval=5E-6
  |OR=149.67
  |ORtxt=[NR] unit decrease
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}