"Fulgent Genetics, Fulgent Genetics"[submitter] AND "GP9"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 13533	NM_000174.5(GP9):c.70T>C (p.Cys24Arg)	GP9 (C24R)	Single nucleotide variant (missense variant)	Bernard Soulier syndrome +1 more	GPathogenic
Select item 13529	NM_000174.5(GP9):c.182A>G (p.Asn61Ser)	GP9 (N61S)	Single nucleotide variant (missense variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 343220	NM_000174.5(GP9):c.368C>T (p.Pro123Leu)	GP9 (P123L)	Single nucleotide variant (missense variant)	Bernard Soulier syndrome +2 more	GUncertain significance

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