{{Rsnum
|rsid=113994121
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ADAMTSL2
|position=133540625
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTSL2
}}{{omim
|id=612277
|rsnum=113994121
|variant=0001
}}{{ClinVar
|rsid=113994121
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=136405747
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=ADAMTSL2:9719
|GENE_NAME=ADAMTSL2
|GENE_ID=9719
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.136405747C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK11168; 612277.0001
|CLNSIG=5
|CLNCUI=C0265287; C0265287
|CLNDBN=Geleophysic dysplasia
|Disease=Geleophysic dysplasia
|CLNACC=RCV000000728.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK11168:C0265287:231050:2623:28557005
}}