{{Rsnum
|rsid=3732782
|Gene=ZNF80
|Chromosome=3
|position=114236317
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=C
|GMAF=0.3223
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=ZNF80
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 13.3 | 42.5 | 44.2
| HCB | 18.7 | 53.0 | 28.4
| JPT | 21.4 | 44.6 | 33.9
| YRI | 2.0 | 23.8 | 74.1
| ASW | 3.6 | 38.2 | 58.2
| CHB | 18.7 | 53.0 | 28.4
| CHD | 19.4 | 52.8 | 27.8
| GIH | 7.1 | 40.4 | 52.5
| LWK | 0.9 | 23.6 | 75.5
| MEX | 16.1 | 50.0 | 33.9
| MKK | 1.9 | 21.9 | 76.1
| TSI | 7.9 | 51.5 | 40.6
| HapMapRevision=28
}}
{{PMID|19217756}} a haplotype containing [[rs3732782]], [[rs905568]], and [[rs7620754]] in the 5' region of [[DRD3]] was associated with Tardive dyskinesia diagnosis

{{GET Evidence
|gene=ZNF80
|aa_change=Asp253Ala
|aa_change_short=D253A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3732782
|overall_frequency_n=7510
|overall_frequency_d=10758
|overall_frequency=0.698085
|n_genomes=53
|n_genomes_annotated=0
|n_haplomes=84
|n_articles=0
|n_articles_annotated=0
|nblosum100=5
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}