List of variants in gene combination HBB, LOC107133510, LOC110006319 reported as likely benign for anemia

Minimum submission review status:		Collection method:
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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.315+16G>C	rs10768683	0.82893
NM_000518.5(HBB):c.*96T>C	rs34029390	0.00283
NM_000518.5(HBB):c.316-70C>G	rs193922560	0.00099
NM_000518.5(HBB):c.316-125A>G	rs63751175	0.00045
NM_000518.5(HBB):c.316-179A>C	rs185607297	0.00009
NM_000518.5(HBB):c.316-150C>G	rs193922556	0.00002
NM_000518.5(HBB):c.*104G>A	rs1564873881	0.00001
NM_000518.5(HBB):c.316-184T>C	rs193922557	0.00001
NM_000518.5(HBB):c.327C>T (p.Asn109=)	rs34933751	0.00001
NM_000518.5(HBB):c.*132+34C>A	rs1277208445
NM_000518.5(HBB):c.402G>A (p.Val134=)	rs113082294
NM_000518.5(HBB):c.402G>C (p.Val134=)	rs113082294

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