{{Rsnum
|rsid=387907111
|Chromosome=4
|position=120821326
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRDM5
|Gene_s=PRDM5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=4
|CLNACC=RCV000024109.1
|CLNALLE=1
|CLNDBN=Brittle cornea syndrome 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280011:614170:90354
|CLNHGVS=NC_000004.11:g.121742481T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614161.0004
|Disease=Brittle cornea syndrome 2
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=121742481
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907111
|GENEINFO=PRDM5:11107
|GENE_ID=11107
|GENE_NAME=PRDM5
}}