rs1562905246, COL1A2

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
0.700 GeneticVariation CLINVAR Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta. 24668929 2014
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
0.700 GeneticVariation CLINVAR Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships. 18996919 2009
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
0.700 GeneticVariation CLINVAR Collagen structure and stability. 19344236 2009
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
0.700 GeneticVariation CLINVAR 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. 17078022 2007
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
0.700 GeneticVariation CLINVAR The human type I collagen mutation database. 9016532 1997
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
0.700 GeneticVariation CLINVAR Crystal and molecular structure of a collagen-like peptide at 1.9 A resolution. 7695699 1994
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
0.700 GeneticVariation CLINVAR Characterization of collagen-like peptides containing interruptions in the repeating Gly-X-Y sequence. 8218237 1993