List of variants in gene FGD4 reported as uncertain significance for not specified

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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_001370298.3(FGD4):c.1777C>A (p.Pro593Thr)	rs138160928	0.00168
NM_001370298.3(FGD4):c.2560G>A (p.Val854Met)	rs61753359	0.00131
NM_001370298.3(FGD4):c.1759A>G (p.Met587Val)	rs201186597	0.00016
NM_001370298.3(FGD4):c.1409A>G (p.Gln470Arg)	rs200149526	0.00005
NM_001370298.3(FGD4):c.319+1G>A	rs1057518446	0.00001
NM_001370298.3(FGD4):c.1509G>T (p.Leu503Phe)	rs1555216969
NM_001370298.3(FGD4):c.166+1G>A
NM_001370298.3(FGD4):c.1839G>A (p.Met613Ile)
NM_001370298.3(FGD4):c.1971C>A (p.Ile657=)	rs61748364

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