HBB Chromosome 11

Hemoglobin subunit beta
398 variants 398 Health Risk

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What This Gene Does
The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. The normal adult hemoglobin tetramer consists of two alpha chains and two beta chains. Mutant beta globin causes sickle cell anemia. Absence of beta chain causes beta-zero-thalassemia. Reduced amounts of detectable beta globin causes beta-plus-thalassemia. The order of the genes in the beta-globin cluster is 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Hemoglobin subunits
Locus Type
gene with protein product
Location
11p15.4
Ensembl
ENSG00000244734
Associated Conditions (181)
HEMOGLOBIN LA DESIRADE
Hb SS disease
Hemoglobinopathy
8 conditions
beta Thalassemia
Beta-thalassemia HBB/LCRB
HBB-related disorder
Fetal hemoglobin quantitative trait locus 1
Hemoglobin E
Inborn genetic diseases
HEMOGLOBIN PYRGOS
Malaria
susceptibility to
HEMOGLOBIN N (BALTIMORE)
HEMOGLOBIN N (JENKINS)
HEMOGLOBIN JENKINS
HEMOGLOBIN HOPKINS 1
HEMOGLOBIN KENWOOD
HEMOGLOBIN G (COPENHAGEN)
HEMOGLOBIN G (SASKATOON)
+161 more conditions
Key Variants
All Variants (398)
RSID Category Clinical Significance Conditions
RS33999427 Health Risk Conflicting classifications of pathogenicity HEMOGLOBIN TAK, Hemoglobinopathy, Beta-thalassemia HBB/LCRB
RS34013622 Health Risk Conflicting classifications of pathogenicity Erythrocytosis, familial, 6
RS34029390 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, HBB-related disorder, beta Thalassemia
RS34126315 Health Risk Conflicting classifications of pathogenicity
RS34196559 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, beta Thalassemia
RS34439278 Health Risk Conflicting classifications of pathogenicity
RS34446260 Health Risk Conflicting classifications of pathogenicity HEMOGLOBIN HIKARI, HEMOGLOBIN HIKARI
RS34483965 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, Beta-thalassemia HBB/LCRB, beta Thalassemia
RS34484056 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS34500389 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, HBB-related disorder, 8 conditions
RS34663314 Health Risk Conflicting classifications of pathogenicity
RS34718174 Health Risk Conflicting classifications of pathogenicity
RS34831026 Health Risk Conflicting classifications of pathogenicity HEMOGLOBIN ATHENS-GEORGIA, 8 conditions, HEMOGLOBIN ATHENS-GEORGIA
RS34999973 Health Risk Conflicting classifications of pathogenicity BETA-PLUS-THALASSEMIA, beta Thalassemia, Beta thalassemia intermedia
RS35262412 Health Risk Conflicting classifications of pathogenicity HEMOGLOBIN G (TEXAS), HEMOGLOBIN G (GALVESTON), HEMOGLOBIN G (PORT ARTHUR)
RS35578002 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, beta Thalassemia
RS35799536 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, Inborn genetic diseases, HBB-related disorder
RS35939430 Health Risk Conflicting classifications of pathogenicity HEMOGLOBIN CRETE, beta Thalassemia, HEMOGLOBIN CRETE
RS36092904 Health Risk Conflicting classifications of pathogenicity
RS369101035 Health Risk Conflicting classifications of pathogenicity
RS370724350 Health Risk Conflicting classifications of pathogenicity
RS374373297 Health Risk Conflicting classifications of pathogenicity
RS386134236 Health Risk Conflicting classifications of pathogenicity
RS397515291 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, beta Thalassemia
RS537944366 Health Risk Conflicting classifications of pathogenicity
RS63750628 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, Hb SS disease, Hemoglobin E
RS63750717 Health Risk Conflicting classifications of pathogenicity
RS63750840 Health Risk Conflicting classifications of pathogenicity HEMOGLOBIN D (OULED RABAH), beta Thalassemia, HEMOGLOBIN D (OULED RABAH)
RS63750953 Health Risk Conflicting classifications of pathogenicity Beta thalassemia intermedia, 8 conditions, Beta thalassemia intermedia
RS63750954 Health Risk Conflicting classifications of pathogenicity BETA-PLUS-THALASSEMIA, beta Thalassemia, Beta-thalassemia HBB/LCRB
RS63751175 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, HBB-related disorder, beta Thalassemia
RS72561473 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, beta Thalassemia
RS753344875 Health Risk Conflicting classifications of pathogenicity
RS769583496 Health Risk Conflicting classifications of pathogenicity beta Thalassemia, Hb SS disease, Fetal hemoglobin quantitative trait locus 1
RS781604042 Health Risk Conflicting classifications of pathogenicity
RS887821047 Health Risk Conflicting classifications of pathogenicity
RS930802593 Health Risk Conflicting classifications of pathogenicity
RS964085975 Health Risk Conflicting classifications of pathogenicity
RS1141387 Health Risk Likely pathogenic Erythrocytosis, familial, 6
RS1420779550 Health Risk Likely pathogenic
RS1554917831 Health Risk Likely pathogenic
RS1554917947 Health Risk Likely pathogenic Beta-thalassemia HBB/LCRB, Beta-thalassemia HBB/LCRB
RS1554918165 Health Risk Likely pathogenic beta Thalassemia, Beta-thalassemia HBB/LCRB, beta Thalassemia
RS1847527770 Health Risk Likely pathogenic
RS1847556466 Health Risk Likely pathogenic
RS193922552 Health Risk Likely pathogenic beta Thalassemia, beta Thalassemia
RS193922553 Health Risk Likely pathogenic Dominant beta-thalassemia, beta Thalassemia, Dominant beta-thalassemia
RS2133587981 Health Risk Likely pathogenic beta Thalassemia, beta Thalassemia
RS2133588176 Health Risk Likely pathogenic beta Thalassemia, Beta-thalassemia HBB/LCRB, beta Thalassemia
RS2133588679 Health Risk Likely pathogenic Hemoglobinopathy, Hemoglobinopathy
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