{{Rsnum
|rsid=116840767
|Chromosome=7
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=GLI3
|position=41965687
|Gene_s=GLI3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=7
|CLNALLE=1
|CLNDBN=Pallister-Hall syndrome
|CLNDSDB=OMIM
|CLNDSDBID=146510
|CLNHGVS=NC_000007.13:g.42005285delA
|CLNORIGIN=0
|CLNSIG=5
|Disease=Pallister-Hall syndrome
|FwdREF=T
|GENEINFO=GLI3:2737
|GENE_ID=2737
|GENE_NAME=GLI3
|REF=CA
|RSPOS=42005283
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168001201000002110200
|WGT=1
|dbSNPBuildID=132
|rsid=116840767
}}{{PMID Auto
|PMID=15739154
|Title=Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
|OA=1
}}