Variants in gene G6PD with conflicting interpretations "other" and "likely pathogenic"

Submission 1 (other) minimum review status:		Submission 1 (other) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000402.4(G6PD):c.632A>T (p.Asp211Val)	rs5030872	0.00048
NM_000402.4(G6PD):c.653C>T (p.Ser218Phe)	rs5030868	0.00028
NM_000402.4(G6PD):c.583A>G (p.Asn195Asp)	rs137852331	0.00004
NM_000402.4(G6PD):c.1114C>T (p.Leu372Phe)	rs137852342	0.00003
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr)	rs76645461	0.00001
NM_000402.4(G6PD):c.1192G>A (p.Glu398Lys)	rs387906468
NM_000402.4(G6PD):c.1406G>C (p.Arg469Pro)	rs137852337
NM_000402.4(G6PD):c.1429G>A (p.Gly477Arg)	rs137852317
NM_000402.4(G6PD):c.482G>T (p.Gly161Val)	rs137852341
NM_000402.4(G6PD):c.727G>T (p.Val243Leu)	rs137852326

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