Variants in gene G6PD with conflicting interpretations "uncertain significance" and "other"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000402.4(G6PD):c.466A>G (p.Asn156Asp)	rs1050829	0.08672
NM_000402.4(G6PD):c.292G>A (p.Val98Met)	rs1050828	0.03616
NM_000402.4(G6PD):c.556G>A (p.Glu186Lys)	rs137852313	0.00014
NM_000402.4(G6PD):c.1114C>T (p.Leu372Phe)	rs137852342	0.00003
NM_000402.4(G6PD):c.1406G>C (p.Arg469Pro)	rs137852337
NM_000402.4(G6PD):c.262G>A (p.Asp88Asn)	rs137852315

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