{{Rsnum
|rsid=10898392
|Gene=DLG2
|Chromosome=11
|position=85453707
|Orientation=plus
|GMAF=0.4362
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=DLG2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 24.8 | 53.1 | 22.1
| HCB | 22.6 | 43.1 | 34.3
| JPT | 26.5 | 44.2 | 29.2
| YRI | 44.2 | 47.6 | 8.2
| ASW | 38.6 | 52.6 | 8.8
| CHB | 22.6 | 43.1 | 34.3
| CHD | 15.6 | 49.5 | 34.9
| GIH | 22.8 | 55.4 | 21.8
| LWK | 36.7 | 53.2 | 10.1
| MEX | 55.2 | 36.2 | 8.6
| MKK | 40.4 | 43.6 | 16.0
| TSI | 20.6 | 53.9 | 25.5
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19570815
|Trait=Height
|Title=A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
|RiskAllele=T
|Pval=0.000003
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10898392
|overall_frequency_n=48
|overall_frequency_d=126
|overall_frequency=0.380952
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=44
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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