Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
BERYLLIUM DISEASE, CHRONIC, SUSCEPTIBILITY TO
CUI: C4016208
Disease: BERYLLIUM DISEASE, CHRONIC, SUSCEPTIBILITY TO
0.700 SusceptibilityMutation CLINVAR
Deuteranomaly
CUI: C3887938
Disease: Deuteranomaly
0.010 GeneticVariation BEFREE One described Human Leukocyte Antigen gene variant, HLA-DP beta 1*0201, contains a substitution of glutamate for lysine at position 69 that appears to have high sensitivity (approximately 94%) but low specificity (approximately 70%) with respect to CBD among individuals occupationally exposed to respirable beryllium. 10795342 2000