{{Rsnum
|rsid=387907334
|Chromosome=3
|position=33120433
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CRTAP
|Gene_s=CRTAP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=3
|CLNACC=RCV000034836.2
|CLNALLE=1
|CLNDBN=Osteogenesis imperfecta type 7
|CLNDSDB=MedGen:OMIM:OMIM
|CLNDSDBID=C1853162:610682:610854
|CLNHGVS=NC_000003.11:g.33161925T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605497.0008
|Disease=Osteogenesis imperfecta type 7
|FwdALT=G
|FwdREF=T
|REF=T
|RSPOS=33161925
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907334
|GENEINFO=CRTAP:10491
|GENE_ID=10491
|GENE_NAME=CRTAP
}}