{{Rsnum
|rsid=387906995
|Chromosome=11
|position=126001812
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CDON
|Gene_s=CDON
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000023726.1
|CLNALLE=1
|CLNDBN=Holoprosencephaly 11
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280215:614226:2162
|CLNHGVS=NC_000011.9:g.125871707G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608707.0001
|Disease=Holoprosencephaly 11
|FwdALT=G
|FwdREF=C
|REF=G
|RSPOS=125871707
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906995
|GENEINFO=CDON:50937
|GENE_ID=50937
|GENE_NAME=CDON
}}