rs281864817, HBA2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hemoglobinopathies
CUI: C0019045
Disease: Hemoglobinopathies
0.010 GeneticVariation BEFREE Haemoglobin Fontainebleau (HBA2: c. 64G>C) in Oman: molecular and haematological characteristics and interaction with various haemoglobinopathies. 28784617 2018