{{Rsnum
|rsid=281860267
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=5
|Orientation=minus
|Gene=CSF1R
|position=150061597
|Gene_s=CSF1R
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=5
|CLNACC=RCV000022686.24
|CLNALLE=1
|CLNDBN=Gliosis, familial progressive subcortical
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK100239:C1857300:221820:313808
|CLNHGVS=NC_000005.9:g.149441160T>C
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK100239; 164770.0003
|Disease=Gliosis
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=149441160
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281860267
|GENEINFO=CSF1R:1436
|GENE_ID=1436
|GENE_NAME=CSF1R
}}