{{Rsnum
|rsid=789560
|Gene=C12orf28
|Chromosome=12
|position=69938047
|Orientation=plus
|GMAF=0.08586
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=MYRFL
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 17.7 | 81.4
| HCB | 0.0 | 14.6 | 85.4
| JPT | 0.0 | 16.8 | 83.2
| YRI | 0.0 | 0.7 | 99.3
| ASW | 1.8 | 7.0 | 91.2
| CHB | 0.0 | 14.6 | 85.4
| CHD | 2.8 | 11.9 | 85.3
| GIH | 0.0 | 5.0 | 95.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 1.7 | 17.2 | 81.0
| MKK | 0.0 | 0.6 | 99.4
| TSI | 1.0 | 18.6 | 80.4
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=18951430
|Trait=Attention-deficit/hyperactivity disorder and conduct disorder
|Title=Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study
|RiskAllele=G
|Pval=0.000007
|OR=NR
|ORtxt=NR
}}

{{PharmGKB
|RSID=rs789560
|Name_s=
|Gene_s=C12orf28
|Feature=
|Evidence=PubMed ID:18951430; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. (Initial Sample Size: 938 affected trios; Replication Sample Size: NR); (Region: 12q15; Reported Gene(s): C12orf28; Risk Allele: rs789560-G); (p-value= 0.000007).This variant is associated with Attention-deficit/hyperactivity disorder and conduct disorder.
|Drugs=
|Drug Classes=
|Diseases=Attention Deficit Disorder with Hyperactivity
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740772
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs789560
|overall_frequency_n=8
|overall_frequency_d=128
|overall_frequency=0.0625
|n_genomes=8
|n_genomes_annotated=0
|n_haplomes=8
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
|n_web_uneval=8
}}

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