{{Rsnum
|rsid=113994102
|Chromosome=18
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CTDP1
|position=79710825
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CTDP1
}}{{omim
|id=604927
|rsnum=113994102
|variant=0001
}}{{ClinVar
|rsid=113994102
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=77470825
|CHROM=18
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050160000000000002110100
|GENEINFO=CTDP1:9150
|GENE_NAME=CTDP1
|GENE_ID=9150
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.77470825C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK25565; 604927.0001
|CLNSIG=5
|CLNCUI=C1858726; C1858726
|CLNDBN=Congenital Cataracts, Facial Dysmorphism, and Neuropathy
|Disease=Congenital Cataracts
|CLNACC=RCV000005622.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK25565:C1858726:604168:48431
}}