{{Rsnum
|rsid=397514461
|Chromosome=Y
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SHOX
|position=640842
|Gene_s=SHOX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=Y
|CLNACC=RCV000022887.2; RCV000022888.2
|CLNALLE=1
|CLNDBN=Leri Weill dyschondrosteosis; Langer mesomelic dysplasia syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1215:CN031459:127300; C0432230:249700:2632:38494008
|CLNHGVS=NC_000023.10:g.601577G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=312865.0014
|Disease=Leri Weill dyschondrosteosis; Langer mesomelic dysplasia syndrome
|FwdALT=C
|FwdREF=G
|GENEINFO=SHOX:6473
|GENE_ID=6473
|GENE_NAME=SHOX
|REF=G
|RSPOS=551577
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514461
}}