"3billion"[submitter] AND "FLG"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1705697	NM_002016.2(FLG):c.9901A>T (p.Arg3301Ter)	FLG, FLG-AS1 (R3301*)	Single nucleotide variant (nonsense)	Dermatitis, atopic, 2	GLikely pathogenic
Select item 280218	NM_002016.2(FLG):c.7487del (p.Thr2496fs)	CCDST, FLG (T2496fs)	Deletion (frameshift variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 522001	NM_002016.2(FLG):c.7031C>G (p.Ser2344Ter)	CCDST, FLG (S2344*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 419605	NM_002016.2(FLG):c.6950_6957del (p.Ala2316_Ser2317insTer)	CCDST, FLG	Deletion (nonsense)	Dermatitis, atopic, 2 +2 more	GPathogenic/Likely pathogenic
Select item 2572530	NM_002016.2(FLG):c.2767dup (p.Ser923fs)	FLG, FLG-AS1 (S923fs)	Duplication (frameshift variant)	Ichthyosis vulgaris	GLikely pathogenic
Select item 16320	NM_002016.2(FLG):c.2282_2285del (p.Ser761fs)	CCDST, FLG (S761fs)	Microsatellite (frameshift variant)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 1345023	NM_002016.2(FLG):c.1714C>T (p.Arg572Ter)	FLG, FLG-AS1 (R572*)	Single nucleotide variant (nonsense)	Ichthyosis vulgaris +1 more	GPathogenic/Likely pathogenic
Select item 16319	NM_002016.2(FLG):c.1501C>T (p.Arg501Ter)	CCDST, FLG (R501*)	Single nucleotide variant (nonsense)	Ichthyosis vulgaris +5 more	GPathogenic/Likely pathogenic

ClinVar