{{Rsnum
|rsid=104894732
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TYROBP
|position=35908227
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYROBP
}}{{omim
|id=604142
|rsnum=104894732
|variant=0003
}}{{ClinVar
|rsid=104894732
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=36399129
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TYROBP:7305
|GENE_NAME=TYROBP
|GENE_ID=7305
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.36399129A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604142.0003
|CLNSIG=5
|CLNCUI=C1857316
|CLNDBN=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|Disease=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|CLNACC=RCV000006153.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1197:C1857316:221770:2770
}}