"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "IL36RN"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 30489	NM_012275.3(IL36RN):c.80T>C (p.Leu27Pro)	IL36RN (L27P)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic
Select item 624147	NM_012275.3(IL36RN):c.115+5G>A	IL36RN	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance
Select item 493284	NM_012275.3(IL36RN):c.169G>A (p.Val57Ile)	IL36RN (V57I)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 575254	NM_012275.3(IL36RN):c.227C>T (p.Pro76Leu)	IL36RN (P76L)	Single nucleotide variant (missense variant)	Generalized pustular psoriasis +1 more	GConflicting classifications of pathogenicity
Select item 529885	NM_012275.3(IL36RN):c.230C>T (p.Thr77Ile)	IL36RN (T77I)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 160374	NM_012275.3(IL36RN):c.304C>T (p.Arg102Trp)	IL36RN (R102W)	Single nucleotide variant (missense variant)	Acrodermatitis continua suppurativa of Hallopeau +1 more	GUncertain significance
Select item 30490	NM_012275.3(IL36RN):c.338C>T (p.Ser113Leu)	IL36RN (S113L)	Single nucleotide variant (missense variant)	Acrodermatitis continua suppurativa of Hallopeau +4 more	GConflicting classifications of pathogenicity

ClinVar