{{Rsnum
|rsid=201227603
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HPS3
|position=149145547
|Gene_s=HPS3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=3
|CLNACC=RCV000004872.1
|CLNALLE=1
|CLNDBN=Hermansky-Pudlak syndrome 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1287:CN068829:614072:231512:79430
|CLNHGVS=NC_000003.11:g.148863334G>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1287; 606118.0002
|Disease=Hermansky-Pudlak syndrome 3
|FwdALT=T
|FwdREF=C
|GENEINFO=HPS3:84343
|GENE_ID=84343
|GENE_NAME=HPS3
|REF=G
|RSPOS=148863334
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=201227603
}}