{{Rsnum
|rsid=386833842
|Chromosome=19
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TYROBP
|position=35907232
|Gene_s=TYROBP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=19
|CLNACC=RCV000049810.1
|CLNALLE=1
|CLNDBN=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1197:C1857316:221770:2770
|CLNHGVS=NC_000019.9:g.36398134C>A
|CLNSIG=4
|Disease=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|FwdALT=T
|FwdREF=G
|REF=C
|RSPOS=36398134
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833842
|GENEINFO=TYROBP:7305
|GENE_ID=7305
|GENE_NAME=TYROBP
}}{{PMID Auto
|PMID=17125796
|Title=A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease.
}}