{{Rsnum
|rsid=386834006
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TRIM37
|position=59064406
|Gene_s=TRIM37
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=17
|CLNACC=RCV000049984.1
|CLNALLE=1
|CLNDBN=Mulibrey nanism syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0524582:253250:2576:81604003
|CLNHGVS=NC_000017.10:g.57141767C>T
|CLNSIG=4
|Disease=Mulibrey nanism syndrome
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=57141767
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386834006
|GENEINFO=TRIM37:4591
|GENE_ID=4591
|GENE_NAME=TRIM37
}}{{PMID Auto
|PMID=12754710
|Title=A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity.
}}