ClinVar for OMIM (Select 601960) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 31609	NM_001366385.1(CARD14):c.413A>C (p.Glu138Ala)	CARD14 (E138A)	Single nucleotide variant (missense variant +1 more)	Psoriasis 2, pustular	GPathogenic
Select item 31606	NM_001366385.1(CARD14):c.349G>A (p.Gly117Ser)	CARD14 (G117S)	Single nucleotide variant (missense variant +1 more)	Pityriasis rubra pilaris +1 more	GPathogenic