Related gene-specific medical variations for Gene (Select 641339) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2690468	NM_001190417.2(ZNF674):c.1540C>A (p.His514Asn)	ZNF674 (H513N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 688167	GRCh37/hg19 Xp11.3-11.23(chrX:46371061-46408859)x2	ZNF674	Copy number gain	not provided	GUncertain significance
Select item 686790	GRCh37/hg19 Xp11.3-11.23(chrX:46371128-46408674)x3	ZNF674	Copy number gain	not provided	GUncertain significance
Select item 686773	GRCh37/hg19 Xp11.3-11.23(chrX:46371061-46408674)x3	ZNF674	Copy number gain	not provided	GUncertain significance
Select item 395159	GRCh37/hg19 Xp11.3-11.23(chrX:46366112-46407858)x2	ZNF674	Copy number gain	See cases	GUncertain significance
Select item 253998	GRCh37/hg19 Xp11.3-11.23(chrX:46366112-46407917)x2	ZNF674	Copy number gain	See cases	GUncertain significance

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