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

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.315+16G>C	rs10768683	0.82893
NM_000518.5(HBB):c.316-185C>T	rs1609812	0.82712
NM_000518.5(HBB):c.315+74T>G	rs7480526	0.44189
NM_000518.5(HBB):c.315+81C>T	rs7946748	0.10445
NM_000518.5(HBB):c.316-373C>A	rs78815705	0.02031
NC_000011.10:g.5225416C>T	rs113969885	0.01596
NM_000518.5(HBB):c.*96T>C	rs34029390	0.00283
NM_000518.5(HBB):c.315+26T>G	rs368604295	0.00234
NM_000518.5(HBB):c.432C>T (p.His144=)	rs36020563	0.00145
NM_000518.5(HBB):c.316-272G>C	rs773343845	0.00006
NM_000518.4(HBB):c.410G>A (p.Gly137Asp)	rs33949486	0.00001
NM_000518.5(HBB):c.315+255T>C	rs1847544780
NM_000518.5(HBB):c.316-208C>G	rs1847537539
NM_000518.5(HBB):c.316-272G>T	rs773343845
NM_000518.5(HBB):c.373C>A (p.Pro125Thr)	rs35461710
NM_000518.5(HBB):c.402G>C (p.Val134=)	rs113082294

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