HBA1, hemoglobin subunit alpha 1, 3039

N. diseases: 200; N. variants: 25
Disease: ERYTHROCYTOSIS, FAMILIAL, 7 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs33935328
rs33935328
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		A 0.700 CausalMutation CLINVAR
dbSNP: rs33935328
rs33935328
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		T 0.700 CausalMutation CLINVAR
dbSNP: rs33978134
rs33978134
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		T 0.700 CausalMutation CLINVAR
dbSNP: rs33986902
rs33986902
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		G 0.700 CausalMutation CLINVAR
dbSNP: rs33991779
rs33991779
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		T 0.700 CausalMutation CLINVAR
dbSNP: rs33991779
rs33991779
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		A 0.700 CausalMutation CLINVAR
dbSNP: rs33991910
rs33991910
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		T 0.700 CausalMutation CLINVAR
dbSNP: rs35239527
rs35239527
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		T 0.700 CausalMutation CLINVAR
dbSNP: rs35723200
rs35723200
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		C 0.700 CausalMutation CLINVAR
dbSNP: rs63750950
rs63750950
Entrez Id: 3039
Gene Symbol: HBA1
HBA1
CUI: C4693823
Disease:
ERYTHROCYTOSIS, FAMILIAL, 7 		C 0.700 CausalMutation CLINVAR