{{Rsnum
|rsid=119471023
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HPS4
|position=26468571
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HPS4
}}{{omim
|id=606682
|rsnum=119471023
|variant=0006
}}{{ClinVar
|rsid=119471023
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=26864537
|CHROM=22
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=HPS4:89781
|GENE_NAME=HPS4
|GENE_ID=89781
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.26864537G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1287; 606682.0006
|CLNSIG=5
|CLNCUI=CN068794; C0079504
|CLNDBN=Hermansky-Pudlak syndrome 4
|Disease=Hermansky-Pudlak syndrome 4
|CLNACC=RCV000004346.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1287:C3484357:614073:231500:79430
}}