{{Rsnum
|rsid=114814747
|Gene=GLI2
|Chromosome=2
|position=120990472
|Orientation=plus
|GMAF=0.005051
|Gene_s=GLI2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=A
|CAF=0.9949; 0.005051
|CHROM=2
|CLNACC=RCV000030731.24
|CLNALLE=1
|CLNDBN=Holoprosencephaly 9
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1835819:610829:2162
|CLNHGVS=NC_000002.11:g.121748048G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=165230.0007
|COMMON=1
|Disease=Holoprosencephaly 9
|FwdALT=A
|FwdREF=G
|GENEINFO=GLI2:2736
|GENE_ID=2736
|GENE_NAME=GLI2
|REF=G
|RSPOS=121748048
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000040416110100
|WGT=0
|dbSNPBuildID=132
|rsid=114814747
}}