{{Rsnum
|rsid=72653170
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=COL1A1
|position=50188908
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COL1A1
}}{{omim
|id=120150
|rsnum=72653170
|variant=0063
}}

{{ClinVar
|rsid=72653170
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=48266269
|CHROM=17
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=COL1A1:1277
|GENE_NAME=COL1A1
|GENE_ID=1277
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.48266269G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK99168; 120150.0063
|CLNSIG=5
|CLNCUI=C0020497
|CLNDBN=Infantile cortical hyperostosis; Prenatal cortical hyperostosis, lethal
|Disease=Infantile cortical hyperostosis; Prenatal cortical hyperostosis
|CLNACC=RCV000018889.22; RCV000018890.26
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK99168:C0020497:114000:1310:24752008; C1861980
}}

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