{{Rsnum
|rsid=121917708
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=GLI2
|position=120978500
|Gene_s=GLI2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=165230
|rsnum=121917708
|variant=0003
}}{{ClinVar
|rsid=121917708
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=121736076
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GLI2:2736
|GENE_NAME=GLI2
|GENE_ID=2736
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.121736076C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=165230.0003
|CLNSIG=5
|CLNCUI=C1835819
|CLNDBN=Holoprosencephaly 9
|Disease=Holoprosencephaly 9
|CLNACC=RCV000014848.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1835819:610829:2162
}}