"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "KCNQ3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 372395	NM_004519.4(KCNQ3):c.2611C>G (p.Pro871Ala)	KCNQ3 (P871A +1 more)	Single nucleotide variant (missense variant)	Seizures, benign familial neonatal, 2 +2 more	GUncertain significance
Select item 449652	NM_004519.4(KCNQ3):c.2545G>A (p.Gly849Ser)	KCNQ3 (G849S +1 more)	Single nucleotide variant (missense variant)	Benign neonatal seizures +1 more	GUncertain significance
Select item 279819	NM_004519.4(KCNQ3):c.1531A>G (p.Met511Val)	KCNQ3 (M511V +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 2683029	NM_004519.4(KCNQ3):c.896A>T (p.Glu299Val)	KCNQ3 (E179V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 934080	NM_004519.4(KCNQ3):c.725G>A (p.Arg242Gln)	KCNQ3 (R122Q +1 more)	Single nucleotide variant (missense variant)	Benign neonatal seizures +1 more	GUncertain significance
Select item 1163893	NM_004519.4(KCNQ3):c.67G>A (p.Gly23Ser)	KCNQ3 (G23S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar