"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC107181 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3036272	NM_001360016.2(G6PD):c.-9+9C>A	G6PD, IKBKG +2 more	Single nucleotide variant (intron variant)	G6PD-related disorder	GLikely benign
Select item 3043617	NM_001360016.2(G6PD):c.-14G>A	G6PD, IKBKG +2 more (S26N)	Single nucleotide variant (missense variant +2 more)	G6PD-related disorder	GBenign
Select item 2628726	NM_001360016.2(G6PD):c.-17G>T	G6PD, IKBKG +2 more (R25L)	Single nucleotide variant (missense variant +2 more)	G6PD-related disorder	GUncertain significance

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