"PreventionGenetics, part of Exact Sciences"[submitter] AND "IRF9"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 781705	NM_006084.5(IRF9):c.87C>T (p.Cys29=)	IRF9	Single nucleotide variant (synonymous variant)	IRF9-related disorder +1 more	GBenign/Likely benign
Select item 1574603	NM_006084.5(IRF9):c.696C>T (p.Gly232=)	IRF9	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1559150	NM_006084.5(IRF9):c.804G>A (p.Thr268=)	IRF9	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign

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