Related gene-specific medical variations for Gene (Select 57507) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3197151	NM_020747.3(ZNF608):c.899C>T (p.Thr300Ile)	LOC129994494, ZNF608 (T300I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1340073	GRCh37/hg19 5q23.2(chr5:123845674-124016425)x1	ZNF608	Copy number loss	not provided	GUncertain significance
Select item 563105	GRCh37/hg19 5q23.2(chr5:123980871-124434498)x3	ZNF608	Copy number gain	not provided	GLikely benign
Select item 563104	GRCh37/hg19 5q23.2(chr5:122957481-124299676)x1	ZNF608	Copy number loss	not provided	GUncertain significance

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