List of variants in gene FGD1 reported as benign by Eurofins NTD LLC (GA)

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_004463.3(FGD1):c.2091T>C (p.Thr697=)	rs12011120	0.17397
NM_004463.3(FGD1):c.2136A>G (p.Pro712=)	rs1126744	0.14669
NM_004463.3(FGD1):c.-4G>C	rs147035080	0.04998
NM_004463.3(FGD1):c.110C>T (p.Ala37Val)	rs75659311	0.00373
NM_004463.3(FGD1):c.676G>A (p.Ala226Thr)	rs138723423	0.00259
NM_004463.3(FGD1):c.2268C>T (p.Cys756=)	rs61734178	0.00217
NM_004463.3(FGD1):c.1617G>A (p.Pro539=)	rs151184308	0.00216
NM_004463.3(FGD1):c.395G>A (p.Arg132Gln)	rs145644275	0.00117
NM_004463.3(FGD1):c.482-10G>A	rs146783766	0.00079

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