List of variants in gene combination HBA2, LOC106804612 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_000517.6(HBA2):c.375C>G (p.Ser125=)	rs775058691	0.00010
NM_000517.6(HBA2):c.414C>T (p.Thr138=)	rs371394396	0.00001

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