Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Low Tension Glaucoma
CUI: C0152136
Disease: Low Tension Glaucoma
0.020 GeneticVariation BEFREE In addition, methylation at CpG sites in CDKN2B was also associated with genotype at rs1063192, which is known to confer risk for NTG. 29265947 2018
Low Tension Glaucoma
CUI: C0152136
Disease: Low Tension Glaucoma
0.020 GeneticVariation BEFREE The rs1063192 (CDKN2B) and rs1900004 (ATOH7) seem to be non-IOP-related genetic risk factors for NTG, and the rs1547014 (CHEK2) is a genetic risk factor for HTG. 22584021 2012