{{Rsnum
|rsid=72656387
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL1A2
|position=94409367
|Gene_s=COL1A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=72656387
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=94038679
|CHROM=7
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050168000000000002100100
|GENEINFO=COL1A2:1278
|GENE_NAME=COL1A2
|GENE_ID=1278
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.94038679G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Osteogenesis imperfecta
|Disease=Osteogenesis imperfecta
|Tags=PM;PMC;SLO;OTHERKG;LSD
|CLNACC=RCV000029613.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1295:C0029434:78314001
}}

{{PMID Auto
|PMID=17078022
|Title=Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.
}}

{{PMID Auto
|PMID=18311573
|Title=Evidence that abnormal high bone mineralization in growing children with osteogenesis imperfecta is not associated with specific collagen mutations.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}