Variants in gene G6PD with conflicting interpretations "benign" and "pathogenic"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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_000402.4(G6PD):c.466A>G (p.Asn156Asp)	rs1050829	0.08672
NM_001360016.2(G6PD):c.486-60C>G	rs2515904	0.04673

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