{{Rsnum
|rsid=267606742
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL1A2
|position=94427628
|Gene_s=COL1A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=7
|CLNACC=RCV000018823.26
|CLNALLE=1
|CLNDBN=Osteogenesis imperfecta type III
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1295:C0268362:259420:666:385483009
|CLNHGVS=NC_000007.13:g.94056940G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120160.0054
|Disease=Osteogenesis imperfecta type III
|FwdALT=A
|FwdREF=G
|GENEINFO=COL1A2:1278
|GENE_ID=1278
|GENE_NAME=COL1A2
|REF=G
|RSPOS=94056940
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606742
}}