{{Rsnum
|rsid=121912907
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=COL1A2
|position=94415263
|Gene_s=COL1A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120160
|rsnum=121912907
|variant=0023
}}{{ClinVar
|rsid=121912907
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=94044575
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=COL1A2:1278
|GENE_NAME=COL1A2
|GENE_ID=1278
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.94044575G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120160.0023; 120160.0038
|CLNSIG=5
|CLNCUI=C0268363; C0268362
|CLNDBN=Osteogenesis imperfecta with normal sclerae, dominant form; Osteogenesis imperfecta type III
|Disease=Osteogenesis imperfecta with normal sclerae; Osteogenesis imperfecta type III
|CLNACC=RCV000018793.22; RCV000018794.26
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1295:C0268363:166220:666:205497004; NBK1295:C0268362:259420:666:385483009
}}