Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs67682641
rs67682641
COL1A1
T 0.700 CausalMutation CLINVAR DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum. 27509835

2016
dbSNP: rs67682641
rs67682641
COL1A1
T 0.700 CausalMutation CLINVAR Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms. 22589248

2012
dbSNP: rs67682641
rs67682641
COL1A1
T 0.700 CausalMutation 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
dbSNP: rs67682641
rs67682641
COL1A1
T 0.700 CausalMutation CLINVAR Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiology. 8094076

1993
dbSNP: rs67682641
rs67682641
COL1A1
T 0.700 CausalMutation CLINVAR An RT-PCR-SSCP screening strategy for detection of mutations in the gene encoding the alpha 1 chain of type I collagen: application to four patients with osteogenesis imperfecta. 7691343

1993
dbSNP: rs67682641
rs67682641
COL1A1
T 0.700 CausalMutation CLINVAR Moderately severe osteogenesis imperfecta associated with substitutions of serine for glycine in the alpha 1(I) chain of type I collagen. 8456809

1993
dbSNP: rs67682641
rs67682641
COL1A1
T 0.700 CausalMutation CLINVAR Characterization of three osteogenesis imperfecta collagen alpha 1(I) glycine to serine mutations demonstrating a position-dependent gradient of phenotypic severity. 1445258

1992