Related gene-specific medical variations for Gene (Select 91603) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259711	NM_052857.4(ZNF830):c.29C>T (p.Pro10Leu)	LOC130060706, ZNF830 (P10L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198672	NM_052857.4(ZNF830):c.185G>A (p.Ser62Asn)	LOC130060706, ZNF830 (S62N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492938	NM_052857.4(ZNF830):c.239C>T (p.Ala80Val)	LOC130060706, ZNF830 (A80V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470810	NM_052857.4(ZNF830):c.178G>A (p.Val60Ile)	LOC130060706, ZNF830 (V60I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458785	NM_052857.4(ZNF830):c.55G>A (p.Glu19Lys)	LOC130060706, ZNF830 (E19K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359212	NM_052857.4(ZNF830):c.128C>T (p.Ala43Val)	LOC130060706, ZNF830 (A43V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328236	NM_052857.4(ZNF830):c.151C>G (p.Leu51Val)	LOC130060706, ZNF830 (L51V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251682	NM_052857.4(ZNF830):c.200A>C (p.Gln67Pro)	LOC130060706, ZNF830 (Q67P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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