{{Rsnum
|rsid=199470476
|Chromosome=10
|position=75028893
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KAT6B
|Gene_s=KAT6B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=10
|CLNACC=RCV000023485.2
|CLNALLE=1
|CLNDBN=Young Simpson syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK114806:C1863557:603736:3047
|CLNHGVS=NC_000010.10:g.76788651G>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605880.0004
|Disease=Young Simpson syndrome
|FwdALT=T
|FwdREF=G
|GENEINFO=KAT6B:23522
|GENE_ID=23522
|GENE_NAME=KAT6B
|REF=G
|RSPOS=76788651
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199470476
}}{{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
}}