HBB, hemoglobin subunit beta, 3043

N. diseases: 272; N. variants: 188
Disease: Beta Thalassemia, Dominant Inclusion Body Type ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs33986703
rs33986703
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C1858990
Disease:
Beta Thalassemia, Dominant Inclusion Body Type 		A 0.700 CausalMutation CLINVAR