{{Rsnum
|rsid=6717918
|Gene=DIS3L2
|Chromosome=2
|position=232290400
|Orientation=plus
|GMAF=0.4683
|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 | 9.1 | 43.6 | 47.3
| HCB | 33.3 | 40.0 | 26.7
| JPT | 36.4 | 50.0 | 13.6
| YRI | 75.9 | 22.4 | 1.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 33.3 | 40.0 | 26.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=6717918
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6717918
|overall_frequency_n=62
|overall_frequency_d=122
|overall_frequency=0.508197
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=56
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}