List of variants in gene FGG reported as pathogenic by NIHR Bioresource Rare Diseases, University of Cambridge

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_021870.2(FGG):c.902G>A (p.Arg301His)	rs121913088	0.00001
NM_021870.2(FGG):c.901C>T (p.Arg301Cys)	rs121913087
NM_021870.3(FGG):c.331A>T (p.Lys111Ter)	rs1578812509

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