"Ambry Genetics"[submitter] AND "IL36RN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1402216	NM_012275.3(IL36RN):c.188G>T (p.Gly63Val)	IL36RN (G63V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2219110	NM_012275.3(IL36RN):c.215T>G (p.Val72Gly)	IL36RN (V72G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 330779	NM_012275.3(IL36RN):c.248T>A (p.Val83Glu)	IL36RN (V83E)	Single nucleotide variant (missense variant)	Generalized pustular psoriasis +1 more	GUncertain significance
Select item 2408855	NM_012275.3(IL36RN):c.313A>G (p.Met105Val)	IL36RN (M105V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1010242	NM_012275.3(IL36RN):c.349C>G (p.Pro117Ala)	IL36RN (P117A)	Single nucleotide variant (missense variant)	Generalized pustular psoriasis +1 more	GUncertain significance
Select item 3109415	NM_012275.3(IL36RN):c.434C>T (p.Pro145Leu)	IL36RN (P145L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar