Related gene-specific medical variations for Gene (Select 55769) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2650395	NM_001396016.1(LOC122539214):c.705G>A (p.Glu235=)	LOC122539214, ZNF83	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2425913	NC_000019.9:g.(?_52714493)_(52716383_?)dup	PPP2R1A, ZNF83	Duplication	not provided	GUncertain significance
Select item 2425912	NC_000019.9:g.(?_52723422)_(52729234_?)dup	PPP2R1A, ZNF83	Duplication	not provided	GUncertain significance
Select item 1513327	NC_000019.9:g.(?_52714493)_(52729234_?)dup	PPP2R1A, ZNF83	Duplication	not provided	GUncertain significance
Select item 1411793	NC_000019.9:g.(?_52693350)_(52693447_?)dup	PPP2R1A, ZNF83	Duplication	not provided	GLikely benign
Select item 156704	NM_018300.4(ZNF83):c.824A>C (p.His275Pro)	ZNF83 (H275P)	Single nucleotide variant (missense variant)	not provided	Gnot provided

ClinVar