{{Rsnum
|rsid=387907110
|Chromosome=4
|position=120695236
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRDM5
|Gene_s=PRDM5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=4
|CLNACC=RCV000024107.1
|CLNALLE=1
|CLNDBN=Brittle cornea syndrome 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280011:614170:90354
|CLNHGVS=NC_000004.11:g.121616391G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614161.0002
|Disease=Brittle cornea syndrome 2
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=121616391
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907110
|GENEINFO=PRDM5:11107
|GENE_ID=11107
|GENE_NAME=PRDM5
}}