{{Rsnum
|rsid=121908906
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AP3B1
|position=78141268
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AP3B1
}}{{omim
|id=603401
|rsnum=121908906
|variant=0007
}}{{ClinVar
|rsid=121908906
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=77437092
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=AP3B1:8546
|GENE_NAME=AP3B1
|GENE_ID=8546
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.77437092G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1287; 603401.0007
|CLNSIG=5
|CLNCUI=C1842362
|CLNDBN=Hermansky Pudlak syndrome 2
|Disease=Hermansky Pudlak syndrome 2
|CLNACC=RCV000006749.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1287:C1842362:608233:79430
}}