{{Rsnum
|rsid=121908316
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HPS3
|position=149150624
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HPS3
}}{{omim
|id=606118
|rsnum=121908316
|variant=0006
}}{{ClinVar
|rsid=121908316
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=148868411
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=HPS3:84343
|GENE_NAME=HPS3
|GENE_ID=84343
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.148868411C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1287; 606118.0006
|CLNSIG=5
|CLNCUI=CN068829
|CLNDBN=Hermansky-Pudlak syndrome 3
|Disease=Hermansky-Pudlak syndrome 3
|CLNACC=RCV000004876.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1287:CN068829:614072:231512:79430
}}