{{Rsnum
|rsid=199470477
|Chromosome=10
|position=75029029
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CT)
|geno3=(CT;CT)
|Gene=KAT6B
|Gene_s=KAT6B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=A
|CHROM=10
|CLNACC=RCV000032258.1
|CLNALLE=1
|CLNDBN=Young Simpson syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK114806:C1863557:603736:3047
|CLNHGVS=NC_000010.10:g.76788787_76788788delCT
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK114806
|Disease=Young Simpson syndrome
|FwdREF=CT
|GENEINFO=KAT6B:23522
|GENE_ID=23522
|GENE_NAME=KAT6B
|REF=ACT
|RSPOS=76788784
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=199470477
}}{{PMID Auto
|PMID=22077973
|Title=Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndrome.
|OA=1
}}