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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000558.5(HBA1):c.95+38C>T	rs556086584	0.00182
NM_000558.5(HBA1):c.250C>T (p.Leu84=)	rs754145030	0.00008
NM_000558.3(HBA1):c.341T>A (p.Leu114His)	rs35654345	0.00001
NM_000558.5(HBA1):c.62A>C (p.His21Pro)	rs33943087	0.00001
NM_000558.5(HBA1):c.63C>A (p.His21Gln)	rs281864502	0.00001
NM_000558.3(HBA1):c.154G>C (p.Gly52Arg)	rs33960522
NM_000558.3(HBA1):c.226G>T (p.Asp76Tyr)	rs33977363
NM_000558.4(HBA1):c.-52C>T	rs1276035978
NM_000558.5(HBA1):c.223G>C (p.Asp75His)	rs28928875
NM_000558.5(HBA1):c.47G>A (p.Gly16Asp)	rs281865560
NM_000558.5(HBA1):c.84G>T (p.Glu28Asp)	rs41530750
NM_000558.5(HBA1):c.91G>A (p.Glu31Lys)	rs33993166

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