List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as benign for anemia

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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: 11

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.5227540G>A	rs10742584	0.96393
NC_000011.10:g.5227411G>A	rs10742583	0.83082
NM_000518.5(HBB):c.9T>C (p.His3=)	rs713040	0.82706
NM_000518.5(HBB):c.93-23T>C	rs111851677	0.00593
NM_000518.5(HBB):c.-31C>T	rs63750628	0.00003
NM_000518.5(HBB):c.262A>C (p.Thr88Pro)	rs35553496	0.00002
NM_000518.4(HBB):c.68A>C (p.Glu23Ala)	rs33936254	0.00001
NM_000518.4(HBB):c.157G>A (p.Asp53Asn)	rs33961886
NM_000518.5(HBB):c.-35A>G	rs1847590703
NM_000518.5(HBB):c.40G>A (p.Ala14Thr)	rs766266418
NM_000518.5(HBB):c.92+13G>T	rs753444453

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