"PreventionGenetics, part of Exact Sciences"[submitter] AND "FCGR2A"[g - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039046	NM_001136219.3(FCGR2A):c.144G>A (p.Pro48=)	FCGR2A	Single nucleotide variant (synonymous variant)	FCGR2A-related disorder	GLikely benign
Select item 3059662	NM_001136219.3(FCGR2A):c.153C>T (p.Asn51=)	FCGR2A	Single nucleotide variant (synonymous variant)	FCGR2A-related disorder	GLikely benign
Select item 402852	NM_001136219.3(FCGR2A):c.187C>T (p.Gln63Ter)	FCGR2A (Q62* +1 more)	Single nucleotide variant (nonsense)	not specified +1 more	GBenign
Select item 402850	NM_001136219.3(FCGR2A):c.188A>G (p.Gln63Arg)	FCGR2A (Q62R +1 more)	Single nucleotide variant (missense variant)	FCGR2A-related disorder +1 more	GBenign

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