{{Rsnum
|rsid=118203985
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ADAMTSL4
|position=150556974
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTSL4
}}{{omim
|id=610113
|rsnum=118203985
|variant=0001
}}{{ClinVar
|rsid=118203985
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=150556974
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=ADAMTSL4:54507
|GENE_NAME=ADAMTSL4
|GENE_ID=54507
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.150556974T>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_019032.5:c.1785T>G; 610113.0001
|CLNSIG=5
|CLNCUI=C2673634
|CLNDBN=Ectopia lentis, isolated autosomal recessive
|Disease=Ectopia lentis
|CLNACC=RCV000001414.1
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK84111:C2673634:225100:ORPHA1885
}}