{{Rsnum
|rsid=137852552
|Chromosome=Y
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SHOX
|position=641037
|Gene_s=SHOX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=312865
|variant=0001
|rsnum=137852552
}}{{ClinVar
|rsid=137852552
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=551772
|CHROM=Y
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=SHOX:6473
|GENE_NAME=SHOX
|GENE_ID=6473
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.601772C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=312865.0001
|CLNSIG=5
|CLNCUI=C1845118
|CLNDBN=Short stature, idiopathic, X-linked
|Disease=Short stature
|CLNACC=RCV000010547.2
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845118:300582:314795
}}{{PMID|17047}} [In memoriam: Dr. Fritz Arndts].

{{PMID|10634394}} Identification of short stature caused by SHOX defects and therapeutic effect of recombinant human growth hormone.

{{PMID|10749976}} The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

{{PMID|11739418}} Phenotypes Associated with SHOX Deficiency.

{{PMID|12362035|OA=1
}} Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood.

{{PMID|17028440}} Unique deletion in exon 5 of SHOX gene in a patient with idiopathic short stature.