{{Rsnum
|rsid=1107946
|Gene=COL1A1
|Chromosome=17
|position=50203629
|Orientation=plus
|GMAF=0.2525
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=COL1A1
}}{{omim
|id=120150
|desc=COLLAGEN, TYPE I, ALPHA-1; COL1A1
|rsnum=1107946
}}

{{omim
|id=120150
|rsnum=1107946
|variant=0067
}}

{{omim
|id=166710
|rsnum=1107946
}}

{{PMID Auto
|PMID=22174012
|Title=JAG1 and COL1A1 polymorphisms and haplotypes in relation to bone mineral density variations in postmenopausal Mexican-Mestizo Women
|OA=1
}}

{{PMID Auto
|PMID=22190259
|Title=COL1A1 haplotypes and hip fracture
}}

{{PMID|15113403|OA=1
}} Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosis.

{{PMID|15157284|OA=1
}} Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes.

{{PMID|16804049}} Haplotypes defined by promoter and intron 1 polymorphisms of the COLIA1 gene regulate bone mineral density in women.

{{PMID|17303000}} Association and linkage analysis of COL1A1 and AHSG gene polymorphisms with femoral neck bone geometric parameters in both Caucasian and Chinese nuclear families.

{{PMID|17557158}} The COL1A1 gene and high myopia susceptibility in Japanese.

{{PMID|17697348|OA=1
}} Technology to accelerate pangenomic scanning for unknown point mutations in exonic sequences: cycling temperature capillary electrophoresis (CTCE).

{{PMID|17903296|OA=1
}} Genome-wide association with bone mass and geometry in the Framingham Heart Study.

{{PMID|18787887|OA=1
}} Genetic variation in candidate osteoporosis genes, bone mineral density, and fracture risk: the study of osteoporotic fractures.

{{PMID|19016596}} A rare haplotype in the upstream regulatory region of COL1A1 is associated with reduced bone quality and hip fracture.

{{PMID|20798928}} Polymorphisms in the 5' flank of COL1A1 gene and osteoporosis: meta-analysis of published studies.

{{PMID|21269451|OA=1
}} Synopsis and meta-analysis of genetic association studies in osteoporosis for the focal adhesion family genes: the CUMAGAS-OSTEOporosis information system.

{{PMID|22057139}} A haplotype derived from the common variants at the -1997G/T and Sp1 binding site of the COL1A1 gene influences risk of postmenopausal osteoporosis in India.

{{PMID|22066665}} Bone mineral density and genetic markers involved in three connected pathways (focal adhesion, actin cytoskeleton regulation and cell cycle): the CUMAGAS-BMD information system.

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