{{Rsnum
|rsid=121912911
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=COL1A2
|position=94426442
|Gene_s=COL1A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120160
|rsnum=121912911
|variant=0037
}}{{ClinVar
|rsid=121912911
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=94055754
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=COL1A2:1278
|GENE_NAME=COL1A2
|GENE_ID=1278
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.94055754G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120160.0037
|CLNSIG=5
|CLNCUI=C0268362
|CLNDBN=Osteogenesis imperfecta type III
|Disease=Osteogenesis imperfecta type III
|CLNACC=RCV000018806.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1295:C0268362:259420:666:385483009
}}