Variants in gene combination G6PD, IKBKG with conflicting interpretations reported as "other and "uncertain significance"

Submission 1 (other) minimum review status:		Submission 1 (other) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001360016.2(G6PD):c.102CAT[2] (p.Ile36del)	rs137852338

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