List of variants in gene FGD4 reported by Inherited Neuropathy Consortium

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001370298.3(FGD4):c.1248-1G>A	rs1592368399
NM_001370298.3(FGD4):c.1248-2A>G	rs1592368395
NM_001370298.3(FGD4):c.1304T>C (p.Met435Thr)	rs63749871
NM_001370298.3(FGD4):c.1304T>G (p.Met435Arg)	rs63749871
NM_001370298.3(FGD4):c.1543+1G>A	rs1592388367
NM_001370298.3(FGD4):c.1736G>A (p.Arg579His)	rs281865063
NM_001370298.3(FGD4):c.2039_2040del (p.Glu680fs)	rs1565921326
NM_001370298.3(FGD4):c.2109G>A (p.Met703Ile)	rs281865064
NM_001370298.3(FGD4):c.2173-2A>G	rs281865065
NM_001370298.3(FGD4):c.2183G>A (p.Trp728Ter)	rs1592488602
NM_001370298.3(FGD4):c.2297_2300del (p.Arg766fs)	rs1592489096
NM_001370298.3(FGD4):c.2298_2302del (p.Lys767fs)	rs751035912
NM_001370298.3(FGD4):c.2301_2305del (p.Lys767fs)	rs1592489165
NM_001370298.3(FGD4):c.925dup (p.Ala309fs)	rs1565869918

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