Related gene-specific medical variations for Gene (Select 53833) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109299	NM_144717.4(IL20RB):c.205G>A (p.Glu69Lys)	IL20RB, IL20RB-AS1 (E69K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595824	NM_144717.4(IL20RB):c.236C>T (p.Thr79Met)	IL20RB, IL20RB-AS1 (T79M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2513526	NM_144717.4(IL20RB):c.176C>T (p.Ala59Val)	IL20RB, IL20RB-AS1 (A59V)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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