List of variants in gene combination CCDST, FLG reported as likely pathogenic by Neuberg Centre For Genomic Medicine, NCGM

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_002016.2(FLG):c.7031C>G (p.Ser2344Ter)	rs372754256	0.00015
NM_002016.2(FLG):c.10919C>G (p.Ser3640Ter)
NM_002016.2(FLG):c.762_766del (p.Lys255fs)

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