List of variants in gene FGD1 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004463.3(FGD1):c.676G>A (p.Ala226Thr)	rs138723423	0.00259
NM_004463.3(FGD1):c.395G>A (p.Arg132Gln)	rs145644275	0.00117
NM_004463.3(FGD1):c.935C>T (p.Pro312Leu)	rs28935498	0.00034
NM_004463.3(FGD1):c.1101+20G>C	rs146079207

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