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

Submission 1 (other) minimum review status:		Submission 1 (other) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000558.3(HBA1):c.154G>A (p.Gly52Ser)	rs33960522	0.00030
NM_000558.3(HBA1):c.341T>A (p.Leu114His)	rs35654345	0.00001
NM_000558.3(HBA1):c.154G>C (p.Gly52Arg)	rs33960522
NM_000558.3(HBA1):c.226G>T (p.Asp76Tyr)	rs33977363
NM_000558.3(HBA1):c.270C>G (p.His90Gln)	rs1061009
NM_000558.3(HBA1):c.272A>C (p.Lys91Thr)	rs33911106
NM_000558.3(HBA1):c.349G>A (p.Glu117Lys)	rs63749882
NM_000558.3(HBA1):c.49A>G (p.Lys17Glu)	rs41407250
NM_000558.5(HBA1):c.163C>G (p.Gln55Glu)	rs35317336
NM_000558.5(HBA1):c.223G>C (p.Asp75His)	rs28928875
NM_000558.5(HBA1):c.24G>C (p.Lys8Asn)	rs34410516
NM_000558.5(HBA1):c.273G>C (p.Lys91Asn)	rs33914470
NM_000558.5(HBA1):c.350A>C (p.Glu117Ala)	rs35932809
NM_000558.5(HBA1):c.84G>T (p.Glu28Asp)	rs41530750
NM_000558.5(HBA1):c.91G>A (p.Glu31Lys)	rs33993166

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