{{Rsnum
|rsid=104893945
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DTNBP1
|position=15627391
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DTNBP1
}}{{omim
|id=607145
|rsnum=104893945
|variant=0001
}}{{ClinVar
|rsid=104893945
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=15627622
|CHROM=6
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=DTNBP1:84062
|GENE_NAME=DTNBP1
|GENE_ID=84062
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.15627622G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1287; 607145.0001
|CLNSIG=5
|CLNCUI=CN068646; C0079504
|CLNDBN=Hermansky-Pudlak syndrome 7
|Disease=Hermansky-Pudlak syndrome 7
|CLNACC=RCV000003601.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1287:C3279756:614076:79430
}}