COL1A1 Chromosome 17

Collagen type I alpha 1 chain
1224 variants 1224 Health Risk

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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
RS111594467 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Osteogenesis imperfecta type I
RS111953130 Health Risk Pathogenic Osteogenesis imperfecta, Nonpapillary renal cell carcinoma, Osteogenesis imperfecta
RS112042777 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta
RS112274185 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type III, Osteogenesis imperfecta type I
RS112830882 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS112838331 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1131691607 Health Risk Pathogenic
RS1131692320 Health Risk Pathogenic Osteogenesis imperfecta type III, Osteogenesis imperfecta type III
RS1135348 Health Risk Pathogenic
RS113984451 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1165573890 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1171968124 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1181095991 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1201602830 Health Risk Pathogenic Multiple epiphyseal dysplasia type 1, Osteogenesis imperfecta, perinatal lethal
RS1213427451 Health Risk Pathogenic Osteogenesis imperfecta type I, Ehlers-Danlos syndrome, Osteogenesis imperfecta type I
RS1223061614 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1228746935 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1239012334 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1248406777 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1298621011 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta with normal sclerae, dominant form
RS1351742344 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, 8 conditions
RS138570309 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1402406091 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1420427521 Health Risk Pathogenic
RS1429658299 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1473458290 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS150572711 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta type I, Osteogenesis imperfecta
RS1555571529 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555571647 Health Risk Pathogenic Osteogenesis imperfecta type I, Infantile cortical hyperostosis, Ehlers-Danlos syndrome
RS1555571874 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, 8 conditions
RS1555571916 Health Risk Pathogenic Osteogenesis imperfecta type I, 8 conditions, Osteogenesis imperfecta type I
RS1555571942 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555572015 Health Risk Pathogenic
RS1555572120 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555572121 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555572125 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta
RS1555572239 Health Risk Pathogenic Osteogenesis imperfecta type I, COL1A1-related disorder, Osteogenesis imperfecta type I
RS1555572249 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555572254 Health Risk Pathogenic Joint hypermobility, Reduced bone mineral density, Osteogenesis imperfecta type I
RS1555572331 Health Risk Pathogenic
RS1555572401 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type III, Osteogenesis imperfecta type I
RS1555572456 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555572537 Health Risk Pathogenic
RS1555572640 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555572656 Health Risk Pathogenic
RS1555572756 Health Risk Pathogenic
RS1555573004 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555573039 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS1555573040 Health Risk Pathogenic
RS1555573288 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
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