{{Rsnum
|rsid=386834144
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TREM2
|position=41159790
|Gene_s=TREM2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=6
|CLNACC=RCV000050138.1
|CLNALLE=1
|CLNDBN=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1197:C1857316:221770:2770
|CLNHGVS=NC_000006.11:g.41127528A>G
|CLNSIG=4
|Disease=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|FwdALT=C
|FwdREF=T
|REF=A
|RSPOS=41127528
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386834144
|GENEINFO=TREM2:54209
|GENE_ID=54209
|GENE_NAME=TREM2
}}{{PMID Auto
|PMID=12080485
|Title=Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype.
|OA=1
}}

{{PMID Auto
|PMID=21834902
|Title=Nasu-Hakola disease with a splicing mutation of TREM2 in a Japanese family.
}}