Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72549387
rs72549387
T 0.800 CausalMutation CLINVAR Screening glaucoma genes in adult glaucoma suggests a multiallelic contribution of CYP1B1 to open-angle glaucoma phenotypes. 22004014

2012

dbSNP: rs72549387
rs72549387
T 0.800 CausalMutation CLINVAR Heterozygous loss-of-function variants in CYP1B1 predispose to primary open-angle glaucoma. 19643970

2010

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Mutations in CYP1B1 cause primary congenital glaucoma by reduction of either activity or abundance of the enzyme. 18470941

2008

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Molecular and clinical evaluation of primary congenital glaucoma in Kuwait. 16490498

2006

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Heterozygous CYP1B1 gene mutations in Spanish patients with primary open-angle glaucoma. 16862072

2006

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Primary congenital glaucoma and Rieger's anomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations. 16735994

2006

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Primary role of CYP1B1 in Indian juvenile-onset POAG patients. 16688110

2006

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. 15475877

2004

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma. 15342693

2004

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador. 15255109

2004

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France. 14635112

2003

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients. 12525557

2003

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Gene symbol: CYP1B1. Disease: glaucoma, primary congenital. 14640114

2003

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Molecular genetics of primary congenital glaucoma in Brazil. 12036985

2002

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. 11774072

2002

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees. 11980847

2002

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma. 11527932

2001

dbSNP: rs72549387
rs72549387
T 0.800 CausalMutation CLINVAR Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly. 11403040

2001

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. 10655546

2000

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Novel compound heterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma. 11184479

2000

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma. 10227395

1999

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1. 9497261

1998

dbSNP: rs72549387
rs72549387
0.800 GeneticVariation UNIPROT Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia. 9463332

1998