{{Rsnum
|rsid=28371720
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Orientation=minus
|Chromosome=22
|position=42524178
|Gene=CYP2D6
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
}}{{PharmGKB
|RSID=rs28371720
|Name_s=CYP2D6*9; CYP2D6:2613-2615delAGA
|Gene_s=CYP2D6
|Feature=Exon
|Evidence=Web Resource:http://www.pharmgkb.org/search/annotatedGene/cyp2d6/variant.jsp#ImportantVariantInformationforCYP2D6-777
|Annotation=Causes deletion of amino acid, K281. Contrary to in vitro results, in vivo study has cast doubt on whether or not this variant leads to reduced function.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=In-Depth
|PharmGKB Accession ID=PA161145189
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}