List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as likely pathogenic for Dominant beta-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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.135del (p.Phe46fs)	rs80356820
NM_000518.5(HBB):c.201del (p.Val68fs)	rs193922553
NM_000518.5(HBB):c.282_283dup (p.Asp95fs)	rs34533941

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