Related gene-specific medical variations for Gene (Select 7625) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259392	NM_003426.4(ZNF74):c.379G>A (p.Gly127Ser)	LOC132090920, ZNF74 (G56S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198070	NM_003426.4(ZNF74):c.421C>G (p.Arg141Gly)	LOC132090920, ZNF74 (A112G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538512	NM_003426.4(ZNF74):c.408G>T (p.Glu136Asp)	LOC132090920, ZNF74 (A108S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507705	NM_003426.4(ZNF74):c.359C>T (p.Ala120Val)	LOC132090920, ZNF74 (A120V +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2327711	NM_003426.4(ZNF74):c.422G>T (p.Arg141Leu)	LOC132090920, ZNF74 (R141L +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2306355	NM_003426.4(ZNF74):c.412A>C (p.Ile138Leu)	LOC132090920, ZNF74 (H109P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar