List of variants reported as uncertain significance for Heinz body anemia; alpha Thalassemia; Hemoglobin H disease; Erythrocytosis, familial, 7

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000517.6(HBA2):c.-59C>T	rs1277780626	0.00251
NM_000517.6(HBA2):c.369C>G (p.His123Gln)	rs41479347	0.00013
NM_000517.6(HBA2):c.307A>C (p.Ser103Arg)	rs41321052
NM_000517.6(HBA2):c.394T>C (p.Ser132Pro)

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