{{Rsnum
|rsid=6718438
|Gene=DIS3L2
|Chromosome=2
|position=232290856
|Orientation=plus
|GMAF=0.4022
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DIS3L2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 2.7 | 44.2 | 53.1
| HCB | 36.5 | 36.5 | 27.0
| JPT | 31.0 | 46.0 | 23.0
| YRI | 39.5 | 46.3 | 14.3
| ASW | 24.6 | 42.1 | 33.3
| CHB | 36.5 | 36.5 | 27.0
| CHD | 23.1 | 52.8 | 24.1
| GIH | 4.0 | 32.7 | 63.4
| LWK | 23.6 | 52.7 | 23.6
| MEX | 13.8 | 53.4 | 32.8
| MKK | 16.0 | 48.1 | 35.9
| TSI | 5.9 | 42.2 | 52.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19570815
|Title=A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
|OA=1
}}

{{omim
|id=613440
|rsnum=6718438
}}

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