Variants in gene PIGN with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_176787.5(PIGN):c.167C>T (p.Ala56Val)	rs61755362	0.01101
NM_176787.5(PIGN):c.2712T>G (p.Phe904Leu)	rs34231046	0.00853
NM_176787.5(PIGN):c.528G>A (p.Thr176=)	rs144304758	0.00291
NM_176787.5(PIGN):c.1617T>C (p.Tyr539=)	rs147306123	0.00282
NM_176787.5(PIGN):c.213G>A (p.Pro71=)	rs370553142	0.00014
NM_176787.5(PIGN):c.1117-1=	rs9959632

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