{{Rsnum
|rsid=116840747
|Chromosome=7
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GLI3
|position=41972378
|Gene_s=GLI3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=7
|CLNACC=RCV000031863.1
|CLNALLE=1
|CLNDBN=Pallister-Hall syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1465:C0265220:146510:672:56677004
|CLNHGVS=NC_000007.13:g.42011977C>A
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1465
|Disease=Pallister-Hall syndrome
|FwdALT=T
|FwdREF=G
|GENEINFO=GLI3:2737
|GENE_ID=2737
|GENE_NAME=GLI3
|REF=C
|RSPOS=42011977
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=116840747
}}{{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
}}