{{Rsnum
|rsid=116840744
|Chromosome=7
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=GLI3
|position=41972417
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GLI3
}}{{omim
|id=165240
|rsnum=116840744
|variant=0002
}}{{ClinVar
|rsid=116840744
|Reversed=1
|FwdREF=G
|FwdALT=
|REF=TC
|ALT=T
|RSPOS=42012015
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=GLI3:2737
|GENE_NAME=GLI3
|GENE_ID=2737
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.42012016delC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1465; 165240.0002
|CLNSIG=5
|CLNCUI=C0265220
|CLNDBN=Pallister-Hall syndrome
|Disease=Pallister-Hall syndrome
|CLNACC=RCV000014825.24
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1465:C0265220:146510:672:56677004
}}{{PMID Auto
|PMID=9054938
|Title=GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
}}

{{PMID Auto
|PMID=9192261
|Title=Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome.
|OA=1
}}