List of variants in gene FGA reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.263T>A (p.Leu88His)	rs77531839	0.00078
NM_021871.4(FGA):c.1072G>A (p.Gly358Arg)	rs201105899	0.00007
NM_000508.5(FGA):c.2414G>C (p.Gly805Ala)	rs1730655687
NM_021871.4(FGA):c.1381T>A (p.Cys461Ser)
NM_021871.4(FGA):c.1718G>T (p.Arg573Leu)	rs78506343
NM_021871.4(FGA):c.1904C>A (p.Ser635Tyr)
NM_021871.4(FGA):c.431_432del (p.Lys144fs)	rs934668242
NM_021871.4(FGA):c.5T>C (p.Phe2Ser)
NM_021871.4(FGA):c.784G>A (p.Glu262Lys)	rs1730730138

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