"PreventionGenetics, part of Exact Sciences"[submitter] AND "GP9"[gene - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 255471	NM_000174.5(GP9):c.132G>A (p.Thr44=)	GP9	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 13529	NM_000174.5(GP9):c.182A>G (p.Asn61Ser)	GP9 (N61S)	Single nucleotide variant (missense variant)	Macrothrombocytopenia +4 more	GPathogenic/Likely pathogenic
Select item 900152	NM_000174.5(GP9):c.236C>T (p.Thr79Ile)	GP9 (T79I)	Single nucleotide variant (missense variant)	GP9-related disorder +2 more	GUncertain significance
Select item 900154	NM_000174.5(GP9):c.423G>A (p.Ala141=)	GP9	Single nucleotide variant (synonymous variant)	GP9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 2635956	NM_000174.5(GP9):c.454G>A (p.Val152Met)	GP9 (V152M)	Single nucleotide variant (missense variant)	GP9-related disorder	GUncertain significance
Select item 1122031	NM_000174.5(GP9):c.459G>A (p.Ala153=)	GP9	Single nucleotide variant (synonymous variant)	GP9-related disorder +1 more	GLikely benign
Select item 2140390	NM_000174.5(GP9):c.462G>C (p.Leu154=)	GP9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1654885	NM_000174.5(GP9):c.465C>T (p.Val155=)	GP9	Single nucleotide variant (synonymous variant)	GP9-related disorder +1 more	GLikely benign
Select item 196227	NM_000174.5(GP9):c.466G>A (p.Ala156Thr)	GP9 (A156T)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 255470	NM_000174.5(GP9):c.*7C>T	GP9	Single nucleotide variant (3 prime UTR variant)	not specified +2 more	GBenign/Likely benign