List of variants in gene KCNQ3 reported as likely pathogenic for not provided

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004519.4(KCNQ3):c.878G>A (p.Gly293Glu)	rs1064795142	0.00003
NM_004519.4(KCNQ3):c.1067C>T (p.Ala356Val)	rs1554627025
NM_004519.4(KCNQ3):c.194G>C (p.Gly65Ala)	rs1822519573
NM_004519.4(KCNQ3):c.569G>A (p.Arg190Gln)	rs796052674
NM_004519.4(KCNQ3):c.797A>G (p.Tyr266Cys)	rs796052677
NM_004519.4(KCNQ3):c.913G>T (p.Asp305Tyr)	rs1085307996
NM_004519.4(KCNQ3):c.917C>T (p.Ala306Val)	rs796052678
NM_004519.4(KCNQ3):c.923G>C (p.Trp308Ser)	rs1064794632
NM_004519.4(KCNQ3):c.933G>A (p.Leu311=)	rs2130133290
NM_004519.4(KCNQ3):c.938C>T (p.Thr313Ile)	rs1826478037
NM_004519.4(KCNQ3):c.971C>T (p.Pro324Leu)
NM_004519.4(KCNQ3):c.989G>A (p.Arg330His)	rs1162306056

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