HBB, hemoglobin subunit beta, 3043

N. diseases: 272; N. variants: 188
Disease: Beta thalassemia intermedia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs33913413
rs33913413
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs33941377
rs33941377
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		C 0.700 CausalMutation CLINVAR
dbSNP: rs33941377
rs33941377
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs33941377
rs33941377
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs33944208
rs33944208
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs33978907
rs33978907
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		G 0.700 CausalMutation CLINVAR
dbSNP: rs34598529
rs34598529
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		C 0.700 CausalMutation CLINVAR
dbSNP: rs34999973
rs34999973
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs36015961
rs36015961
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0472767
Disease:
Beta thalassemia intermedia 		G 0.700 CausalMutation CLINVAR