List of variants in gene combination HBB, LOC107133510, LOC110006319 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.*96T>C	rs34029390	0.00283
NM_000518.5(HBB):c.432C>T (p.His144=)	rs36020563	0.00145
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.324C>T (p.Gly108=)	rs193922562	0.00029
NM_000518.5(HBB):c.316-150C>G	rs193922556	0.00002
NM_000518.4(HBB):c.410G>A (p.Gly137Asp)	rs33949486	0.00001
NM_000518.4(HBB):c.430C>T (p.His144Tyr)	rs33929415	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.316-112A>G	rs1847535052
NM_000518.5(HBB):c.351T>C (p.His117=)	rs35209776
NM_000518.5(HBB):c.372C>A (p.Thr124=)	rs780307221
NM_000518.5(HBB):c.372C>G (p.Thr124=)
NM_000518.5(HBB):c.372C>T (p.Thr124=)	rs780307221
NM_000518.5(HBB):c.397A>C (p.Lys133Gln)	rs33953406
NM_000518.5(HBB):c.402G>C (p.Val134=)	rs113082294

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