Related gene-specific medical variations for Gene (Select 7592) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2690465	NM_001324144.2(ZNF41):c.87dup (p.Glu30Ter)	ZNF41 (E30* +4 more)	Duplication (nonsense +1 more)	not provided	GUncertain significance
Select item 2690464	NM_001324144.2(ZNF41):c.1596del (p.Phe532fs)	ZNF41 (F446fs +7 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 145448	GRCh38/hg38 Xp11.3(chrX:47470810-47475689)x1	ZNF41	Copy number loss	See cases	Gconflicting data from submitters
Select item 144506	GRCh38/hg38 Xp11.3(chrX:47470813-47475828)x0	ZNF41	Copy number loss	See cases	GUncertain significance
Select item 144505	GRCh38/hg38 Xp11.3(chrX:47470813-47475828)x1	ZNF41	Copy number loss	See cases	GLikely benign

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