List of variants in gene FCGR2A reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001136219.3(FCGR2A):c.500A>G (p.His167Arg)	rs1801274	0.50935
NM_001136219.3(FCGR2A):c.188A>G (p.Gln63Arg)	rs9427398	0.10243
NM_001136219.3(FCGR2A):c.365-11G>A	rs7529425	0.09887
NM_001136219.3(FCGR2A):c.187C>T (p.Gln63Ter)	rs9427397	0.08981
NM_001136219.3(FCGR2A):c.645A>G (p.Pro215=)	rs11810143	0.08818
NM_001136219.3(FCGR2A):c.879C>T (p.Pro293=)	rs12029217	0.08621

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