{{Rsnum
|rsid=281865471
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=KANSL1
|position=46033131
|Gene_s=KANSL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=17
|CLNACC=RCV000024372.2
|CLNALLE=1
|CLNDBN=17q21.31 microdeletion syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK24676:C1864871:610443:96169
|CLNHGVS=NC_000017.10:g.44110497_44110498delCT
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK24676; 612452.0002
|Disease=17q21.31 microdeletion syndrome
|FwdREF=AG
|REF=CCT
|RSPOS=44110496
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050160000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281865471
|GENEINFO=KANSL1:284058
|GENE_ID=284058
|GENE_NAME=KANSL1
}}