{{Rsnum
|rsid=874426
|Gene=NAV2
|Chromosome=11
|position=19548016
|Orientation=minus
|GMAF=0.3912
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=NAV2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 3.5 | 34.5 | 61.9
| HCB | 33.6 | 48.2 | 18.2
| JPT | 42.5 | 43.4 | 14.2
| YRI | 37.4 | 50.3 | 12.2
| ASW | 24.6 | 54.4 | 21.1
| CHB | 33.6 | 48.2 | 18.2
| CHD | 34.9 | 40.4 | 24.8
| GIH | 5.0 | 44.6 | 50.5
| LWK | 33.6 | 50.9 | 15.5
| MEX | 12.1 | 41.4 | 46.6
| MKK | 30.1 | 48.1 | 21.8
| TSI | 0.0 | 24.5 | 75.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18937294
|Trait=Attention deficit hyperactivity disorder (time to onset)
|Title=Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder
|RiskAllele=C
|Pval=0.000004
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID|20145962|OA=1
}} Molecular genetics of attention-deficit/hyperactivity disorder: an overview.

{{PMID|20148275|OA=1
}} Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs874426
|overall_frequency_n=76
|overall_frequency_d=128
|overall_frequency=0.59375
|n_genomes=45
|n_genomes_annotated=0
|n_haplomes=59
|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}}