"Illumina Laboratory Services, Illumina"[submitter] AND "FLG"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 50930	NM_002016.2(FLG):c.9740C>A (p.Ser3247Ter)	FLG, FLG-AS1 (S3247*)	Single nucleotide variant (nonsense)	FLG-related disorders +4 more	GPathogenic/Likely pathogenic
Select item 50932	NM_002016.2(FLG):c.7339C>T (p.Arg2447Ter)	CCDST, FLG (R2447*)	Single nucleotide variant (nonsense)	FLG-related disorders +3 more	GPathogenic/Likely pathogenic
Select item 265156	NM_002016.2(FLG):c.2476C>T (p.Arg826Ter)	CCDST, FLG (R826*)	Single nucleotide variant (nonsense)	Dermatitis, atopic, 2 +4 more	GConflicting classifications of pathogenicity
Select item 16320	NM_002016.2(FLG):c.2282_2285del (p.Ser761fs)	CCDST, FLG (S761fs)	Microsatellite (frameshift variant)	FLG-related disorders +5 more	GPathogenic/Likely pathogenic
Select item 16319	NM_002016.2(FLG):c.1501C>T (p.Arg501Ter)	CCDST, FLG (R501*)	Single nucleotide variant (nonsense)	FLG-related disorders +6 more	GPathogenic/Likely pathogenic
Select item 280469	NM_002016.2(FLG):c.94G>T (p.Glu32Ter)	CCDST, FLG (E32*)	Single nucleotide variant (nonsense)	FLG-related condition +3 more	GPathogenic/Likely pathogenic

ClinVar