RS80356821 HBB
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What This Variant Does
"CLNSIG=5
Associated Conditions
Beta zero thalassemia
beta Thalassemia
Hb SS disease
Fetal hemoglobin quantitative trait locus 1
Inborn genetic diseases
Beta-thalassemia HBB/LCRB
HBB-related disorder
8 conditions
Hereditary persistence of fetal hemoglobin
Dominant beta-thalassemia
Beta zero thalassemia
beta Thalassemia
Hb SS disease
Fetal hemoglobin quantitative trait locus 1
Inborn genetic diseases
Other Variants in HBB