Related gene-specific medical variations for Gene (Select 65988) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3478186	NM_001305018.2(ZNF747):c.223G>A (p.Ala75Thr)	LOC130058843, ZNF747 (A75T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3478185	NM_001305018.2(ZNF747):c.214C>T (p.His72Tyr)	LOC130058843, ZNF747 (H72Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance