"OMIM"[submitter] AND "IL36RN"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 40007	NM_012275.3(IL36RN):c.28C>T (p.Arg10Ter)	IL36RN (R10*)	Single nucleotide variant (nonsense)	Generalized pustular psoriasis	GUncertain significance
Select item 30489	NM_012275.3(IL36RN):c.80T>C (p.Leu27Pro)	IL36RN (L27P)	Single nucleotide variant (missense variant)	Generalized pustular psoriasis +1 more	GPathogenic
Select item 160373	NM_012275.3(IL36RN):c.104A>G (p.Lys35Arg)	IL36RN (K35R)	Single nucleotide variant (missense variant)	Generalized pustular psoriasis	GUncertain significance
Select item 40005	NM_012275.3(IL36RN):c.115+6T>C	IL36RN	Single nucleotide variant (intron variant)	Acrodermatitis continua suppurativa of Hallopeau +2 more	GPathogenic/Likely pathogenic
Select item 30491	NM_012275.3(IL36RN):c.142C>T (p.Arg48Trp)	IL36RN (R48W)	Single nucleotide variant (missense variant)	Generalized pustular psoriasis	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)	Autoinflammatory syndrome +3 more	GConflicting classifications of pathogenicity
Select item 40006	NM_012275.3(IL36RN):c.368C>G (p.Thr123Arg)	IL36RN (T123R)	Single nucleotide variant (missense variant)	Acrodermatitis continua suppurativa of Hallopeau	GPathogenic