List of variants in gene combination HBA2, LOC106804612 reported as uncertain significance for Heinz body anemia; alpha Thalassemia; Hemoglobin H disease; Erythrocytosis, familial, 7

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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

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