Variants in gene combination HBA1, LOC106804613 with conflicting interpretations reported as "other and "benign"

Submission 1 (other) minimum review status:		Submission 1 (other) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_000558.5(HBA1):c.362C>A (p.Ala121Glu)	rs63749927	0.00001
NM_000558.5(HBA1):c.163C>G (p.Gln55Glu)	rs35317336

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