List of variants in gene KCNQ3 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_004519.4(KCNQ3):c.1994C>T (p.Ser665Leu)	rs147173555	0.00165
NM_004519.4(KCNQ3):c.1885G>C (p.Val629Leu)	rs185511111	0.00016
NM_004519.4(KCNQ3):c.1226C>G (p.Pro409Arg)	rs149272208	0.00009
NM_004519.4(KCNQ3):c.2614A>G (p.Ile872Val)	rs199682667	0.00006
NM_004519.4(KCNQ3):c.1178T>C (p.Ile393Thr)	rs201814804	0.00003
NM_004519.4(KCNQ3):c.73G>A (p.Ala25Thr)	rs1280461599	0.00001
NM_004519.4(KCNQ3):c.1249_1250delinsAT (p.Glu417Met)	rs1554625699
NM_004519.4(KCNQ3):c.2295C>A (p.Asp765Glu)	rs201183533

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