{{Rsnum
|rsid=591044
|Gene=SEZ6L
|Chromosome=22
|position=26301229
|Orientation=plus
|GMAF=0.3848
|Gene_s=SEZ6L
|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 | 17.9 | 52.7 | 29.5
| HCB | 1.5 | 18.2 | 80.3
| JPT | 0.9 | 16.8 | 82.3
| YRI | 44.2 | 44.2 | 11.6
| ASW | 26.3 | 61.4 | 12.3
| CHB | 1.5 | 18.2 | 80.3
| CHD | 1.9 | 14.8 | 83.3
| GIH | 5.0 | 22.8 | 72.3
| LWK | 48.2 | 47.3 | 4.5
| MEX | 6.9 | 41.4 | 51.7
| MKK | 53.2 | 40.4 | 6.4
| TSI | 21.6 | 49.0 | 29.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21901158
|Trait=None
|Title=Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
|RiskAllele=A
|Pval=0.000006
|OR=9.0000
|ORtxt=[5.00 - 13.00] % increase
|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}}