COL1A1 Chromosome 17

Collagen type I alpha 1 chain
1224 variants 1224 Health Risk

Upload your DNA to see your personal genotypes for variants in COL1A1.

What This Gene Does
This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]
Gene Info
Gene Group
Fibrillar collagens
Locus Type
gene with protein product
Location
17q21.33
Ensembl
ENSG00000108821
Associated Conditions (67)
Bone mineral density variation quantitative trait locus
Osteogenesis imperfecta type I
Cardiovascular phenotype
Osteogenesis imperfecta
Infantile cortical hyperostosis
Ehlers-Danlos syndrome
arthrochalasia type
See cases
COL1A1-related disorder
Connective tissue disorder
2
Familial thoracic aortic aneurysm and aortic dissection
8 conditions
7 conditions
Hypertrophic cardiomyopathy
Keratoconus
Osteogenesis imperfecta with normal sclerae
dominant form
Colon adenocarcinoma
Familial cancer of breast
+47 more conditions
Key Variants
RS1107946
association
Bone mineral density variation quantitative trait locus, Bone mineral density variation quantitative trait locus
Health Risk
RS11327935
association
Bone mineral density variation quantitative trait locus, Bone mineral density variation quantitative trait locus
Health Risk
RS1800012
association
Bone mineral density variation quantitative trait locus, Bone mineral density variation quantitative trait locus
Health Risk
RS1009435359
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
Health Risk
RS1014402681
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
Health Risk
RS1033263382
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Cardiovascular phenotype, Osteogenesis imperfecta type I
Health Risk
RS1051473344
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Osteogenesis imperfecta, Infantile cortical hyperostosis
Health Risk
RS1061970
Conflicting classifications of pathogenicity
Infantile cortical hyperostosis, Ehlers-Danlos syndrome, arthrochalasia type
Health Risk
RS113950465
Conflicting classifications of pathogenicity
Osteogenesis imperfecta, Osteogenesis imperfecta type I, Cardiovascular phenotype
Health Risk
RS115997082
Conflicting classifications of pathogenicity
Ehlers-Danlos syndrome, arthrochalasia type, Infantile cortical hyperostosis
Health Risk
RS117672175
Conflicting classifications of pathogenicity
Osteogenesis imperfecta, Ehlers-Danlos syndrome, arthrochalasia type
Health Risk
RS1176922412
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Osteogenesis imperfecta type I, Cardiovascular phenotype
Health Risk
All Variants (1224)
RSID Category Clinical Significance Conditions
RS57377812 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta
RS66489346 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS66490707 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta with normal sclerae, dominant form
RS66511271 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS66523073 Health Risk Pathogenic Osteogenesis imperfecta type III, COL1A1-related disorder, Osteogenesis imperfecta type III
RS66555264 Health Risk Pathogenic Osteogenesis imperfecta type I, 7 conditions, Osteogenesis imperfecta
RS66721653 Health Risk Pathogenic Osteogenesis imperfecta with normal sclerae, dominant form, Osteogenesis imperfecta type I
RS66929517 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta type I
RS66929519 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS67047253 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS67047255 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS67163049 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, perinatal lethal
RS67163050 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS67364703 Health Risk Pathogenic Osteogenesis imperfecta with normal sclerae, dominant form, Osteogenesis imperfecta with normal sclerae
RS67368147 Health Risk Pathogenic Osteogenesis imperfecta type III, Osteogenesis imperfecta with normal sclerae, dominant form
RS67416837 Health Risk Pathogenic
RS67445413 Health Risk Pathogenic Osteogenesis imperfecta type III, Osteogenesis imperfecta type I, See cases
RS67543897 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS67569268 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS67682641 Health Risk Pathogenic Osteogenesis imperfecta type III, Osteogenesis imperfecta type I, Osteogenesis imperfecta with normal sclerae
RS67693970 Health Risk Pathogenic Osteogenesis imperfecta with normal sclerae, dominant form, Osteogenesis imperfecta type I
RS67771061 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta type I, perinatal lethal
RS67879854 Health Risk Pathogenic Osteogenesis imperfecta type I, 7 conditions, COL1A1-related disorder
RS67965462 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS68062484 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS68181175 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta with normal sclerae, dominant form
RS72645315 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645317 Health Risk Pathogenic
RS72645318 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Osteogenesis imperfecta with normal sclerae
RS72645319 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta
RS72645320 Health Risk Pathogenic Osteogenesis imperfecta type III, Osteogenesis imperfecta type III, Osteogenesis imperfecta type III
RS72645321 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, 8 conditions
RS72645323 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta type I, Osteogenesis imperfecta
RS72645324 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645329 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645331 Health Risk Pathogenic Osteogenesis imperfecta type I, Infantile cortical hyperostosis, Osteogenesis imperfecta type I
RS72645332 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645333 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72645334 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645338 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645339 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645341 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Osteogenesis imperfecta type I
RS72645345 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645350 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72645353 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645355 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, perinatal lethal
RS72645356 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72645357 Health Risk Pathogenic Osteogenesis imperfecta type III, Osteogenesis imperfecta, Osteogenesis imperfecta with normal sclerae
RS72645358 Health Risk Pathogenic
RS72645364 Health Risk Pathogenic Osteogenesis imperfecta type I, Uterine corpus endometrial carcinoma, Osteogenesis imperfecta type I
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