{{Rsnum
|rsid=387907333
|Chromosome=3
|position=33114195
|Orientation=plus
|geno1=(GAGCTGATGCCGCTCG;GAGCTGATGCCGCTCG)
|geno2=(GAGCTGATGCCGCTCG;TACCC)
|geno3=(TACCC;TACCC)
|Gene=CRTAP
|Gene_s=CRTAP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CTACCC
|CHROM=3
|CLNACC=RCV000034835.2
|CLNALLE=1
|CLNDBN=Osteogenesis imperfecta type 7
|CLNDSDB=MedGen:OMIM:OMIM
|CLNDSDBID=C1853162:610682:610854
|CLNHGVS=NC_000003.11:g.33155687_33155702del16insTACCC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605497.0007
|Disease=Osteogenesis imperfecta type 7
|FwdALT=TACCC
|FwdREF=GAGCTGATGCCGCTCG
|REF=CGAGCTGATGCCGCTCG
|RSPOS=33155686
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387907333
|GENEINFO=CRTAP:10491
|GENE_ID=10491
|GENE_NAME=CRTAP
}}