"Fulgent Genetics, Fulgent Genetics"[submitter] AND "KRT10-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14576	NM_000421.5(KRT10):c.466C>T (p.Arg156Cys)	KRT10, KRT10-AS1 (R156C)	Single nucleotide variant (missense variant)	Annular epidermolytic ichthyosis +5 more	GPathogenic
Select item 66171	NM_000421.5(KRT10):c.376G>A (p.Gly126Ser)	KRT10, KRT10-AS1 (G126S)	Single nucleotide variant (missense variant)	Epidermolytic ichthyosis +3 more	GBenign/Likely benign
Select item 1186831	NM_000421.5(KRT10):c.49GGA[9] (p.Gly24dup)	KRT10-AS1, KRT10	Microsatellite (inframe_insertion)	not provided +3 more	GLikely benign

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ClinVar