List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as pathogenic for Dominant beta-thalassemia; Heinz body anemia; Hb SS disease; alpha Thalassemia; Malaria, susceptibility to; METHEMOGLOBINEMIA, BETA TYPE; Erythrocytosis, familial, 6; Hereditary persistence of fetal hemoglobin; Beta-thalassemia HBB/LCRB

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.75T>A (p.Gly25=)	rs33951465	0.00006
NM_000518.5(HBB):c.92+2T>C	rs33956879	0.00001
NM_000518.5(HBB):c.-137C>G	rs33941377
NM_000518.5(HBB):c.184A>T (p.Lys62Ter)	rs33995148
NM_000518.5(HBB):c.203_204del (p.Val68fs)	rs34282684

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