"Ambry Genetics"[submitter] AND "CD9"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140707	NM_001769.4(CD9):c.286C>T (p.Leu96Phe)	CD9 (L123F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518269	NM_001769.4(CD9):c.307G>C (p.Glu103Gln)	CD9 (E102Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140708	NM_001769.4(CD9):c.629G>C (p.Gly210Ala)	CD9 (G141A +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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