List of variants in gene HBG1 reported as likely benign for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000559.3(HBG1):c.364G>A (p.Glu122Lys)	rs33963857	0.00006
NM_000559.3(HBG1):c.377A>C (p.Glu126Ala)	rs770330940	0.00004

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