Related gene-specific medical variations for Gene (Select 155061) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198090	NM_001394198.1(ZNF746):c.71A>G (p.Lys24Arg)	LOC126860222, ZNF746 (K24R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198085	NM_001394198.1(ZNF746):c.29C>T (p.Ser10Phe)	LOC126860222, ZNF746 (S10F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198084	NM_001394198.1(ZNF746):c.290G>A (p.Arg97Gln)	LOC126860222, ZNF746 (R97Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617961	NM_001394198.1(ZNF746):c.266G>A (p.Arg89His)	LOC126860222, ZNF746 (R89H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470013	NM_001394198.1(ZNF746):c.223G>A (p.Gly75Arg)	LOC126860222, ZNF746 (G75R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402769	NM_001394198.1(ZNF746):c.169G>A (p.Gly57Arg)	LOC126860222, ZNF746 (G57R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348244	NM_001394198.1(ZNF746):c.73A>G (p.Ile25Val)	LOC126860222, ZNF746 (I25V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348243	NM_001394198.1(ZNF746):c.22C>T (p.Pro8Ser)	LOC129999563, ZNF746 (P8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar