{{Rsnum
|rsid=144372453
|Gene=GLI2
|Chromosome=2
|position=120990577
|Orientation=plus
|GMAF=0.001377
|Gene_s=GLI2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=C
|CAF=0.9986; 0.001377
|CHROM=2
|CLNACC=RCV000030728.24
|CLNALLE=1
|CLNDBN=Holoprosencephaly 9
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1835819:610829:2162
|CLNHGVS=NC_000002.11:g.121748153T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=165230.0004
|COMMON=0
|Disease=Holoprosencephaly 9
|FwdALT=C
|FwdREF=T
|GENEINFO=GLI2:2736
|GENE_ID=2736
|GENE_NAME=GLI2
|REF=T
|RSPOS=121748153
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000040016110100
|WGT=0
|dbSNPBuildID=134
|rsid=144372453
}}