List of variants reported as benign for alpha thalassemia

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000517.6(HBA2):c.-43G>C	rs71382271	1.00000
NM_000517.6(HBA2):c.*107A>G	rs2541640	0.99433
NM_000517.4(HBA2):c.*136A>G	rs2685121	0.86184
NM_000518.5(HBB):c.9T>C (p.His3=)	rs713040	0.82706
NM_000517.6(HBA2):c.-24C>G	rs772829778	0.06872
NM_000558.5(HBA1):c.-24C>G	rs374054030	0.04854
NM_000558.5(HBA1):c.300+55G>T	rs148228241	0.01925
NM_000517.6(HBA2):c.300+55T>G	rs2362746	0.01848
NM_000558.5(HBA1):c.95+39C>T	rs577938658	0.01700
NM_000558.5(HBA1):c.*46C>A	rs141514155	0.01440
NM_000558.5(HBA1):c.-42C>T	rs370305736	0.00968
NM_000517.6(HBA2):c.414C>T (p.Thr138=)	rs371394396	0.00001
NC_000016.10:g.172832C>A	rs1596569257
NC_000016.10:g.176177_176301del	rs1902124319
NM_000517.6(HBA2):c.245C>T (p.Ser82Phe)	rs281864864
NM_000517.6(HBA2):c.301-24delinsCTCGGCCC	rs1596570272
NM_000517.6(HBA2):c.95+11_95+34del	rs1445188229

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