Related gene-specific medical variations for Gene (Select 9861) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2559710	NM_014814.3(PSMD6):c.1075C>A (p.Pro359Thr)	PSMD6, PSMD6-AS2 (P321T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374128	NM_014814.3(PSMD6):c.1021G>A (p.Gly341Arg)	PSMD6, PSMD6-AS2 (G303R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 930281	NM_014814.3(PSMD6):c.146-278_146-277insAAGA	PSMD6 (N49fs)	Insertion (frameshift variant +1 more)	See cases	GUncertain significance

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