{{Rsnum
|rsid=116840768
|Chromosome=7
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GLI3
|position=41965634
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GLI3
}}{{omim
|id=165240
|rsnum=116840768
|variant=0006
}}{{ClinVar
|rsid=116840768
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=42005232
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=GLI3:2737
|GENE_NAME=GLI3
|GENE_ID=2737
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.42005232C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1465; 165240.0006
|CLNSIG=5
|CLNCUI=C0265220
|CLNDBN=Pallister-Hall syndrome
|Disease=Pallister-Hall syndrome
|CLNACC=RCV000014829.24
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1465:C0265220:146510:672:56677004
}}{{PMID|10441570|OA=1
}} The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.