Variants in gene KCNQ3 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 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.2330G>A (p.Arg777Gln)	rs201328910	0.00034
NM_004519.4(KCNQ3):c.2462A>G (p.Asn821Ser)	rs118192254	0.00021
NM_004519.4(KCNQ3):c.954C>A (p.Gly318=)	rs143224896	0.00009
NM_004519.4(KCNQ3):c.1935A>G (p.Gln645=)	rs587781011	0.00008
NM_004519.4(KCNQ3):c.-139dup	rs879019805
NM_004519.4(KCNQ3):c.-140_-139dup	rs879019805
NM_004519.4(KCNQ3):c.-148_-147insTG	rs886062698

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