Variants in gene SERPINA1 with conflicting interpretations "benign" and "other"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (other) minimum review status:		Submission 2 (other) 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_001127701.1(SERPINA1):c.1200A>C (p.Glu400Asp)	rs1303	0.21786
NM_001127701.1(SERPINA1):c.374G>A (p.Arg125His)	rs709932	0.12614

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