{{Rsnum
|rsid=387907198
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=IRX5
|position=54932696
|Gene_s=IRX5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNACC=RCV000024602.1
|CLNALLE=1
|CLNDBN=Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1970027:611174:314555
|CLNHGVS=NC_000016.9:g.54966608G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606195.0002
|Disease=Hypertelorism
|FwdALT=C
|FwdREF=G
|REF=G
|RSPOS=54966608
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907198
|GENEINFO=IRX5:10265
|GENE_ID=10265
|GENE_NAME=IRX5
}}