{{Rsnum
|rsid=281865468
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KANSL1
|position=46171228
|Gene_s=KANSL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000024373.1
|CLNALLE=1
|CLNDBN=17q21.31 microdeletion syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK24676:C1864871:610443:96169
|CLNHGVS=NC_000017.10:g.44248594G>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK24676; 612452.0003
|Disease=17q21.31 microdeletion syndrome
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=44248594
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281865468
|GENEINFO=KANSL1:284058
|GENE_ID=284058
|GENE_NAME=KANSL1
}}