List of variants in gene KCNQ4 reported as likely benign by GeneDx

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.1293-114C>T	rs78213219	0.02616
NM_004700.4(KCNQ4):c.-14G>T	rs886042324	0.00867
NM_004700.4(KCNQ4):c.1614-269C>T	rs79689434	0.00835
NM_004700.4(KCNQ4):c.1614-329A>G	rs116187615	0.00674
NM_004700.4(KCNQ4):c.708+139C>G	rs547528751	0.00637
NM_004700.4(KCNQ4):c.314+38C>T	rs79364948	0.00558
NM_004700.4(KCNQ4):c.1042-52G>A	rs115640797	0.00525
NM_004700.4(KCNQ4):c.1746-284C>A	rs143143085	0.00477
NM_004700.4(KCNQ4):c.1746-283T>G	rs147489203	0.00444
NM_004700.4(KCNQ4):c.946-35C>T	rs143807215	0.00373
NM_004700.4(KCNQ4):c.1614-318C>T	rs137980397	0.00339
NM_004700.4(KCNQ4):c.834+34C>G	rs146642553	0.00331
NM_004700.4(KCNQ4):c.1513+28C>G	rs181431046	0.00269
NM_004700.4(KCNQ4):c.1513+36G>A	rs59037556	0.00246
NM_004700.4(KCNQ4):c.1041+32C>G	rs112135594	0.00235
NM_004700.4(KCNQ4):c.1188C>T (p.Pro396=)	rs189541861	0.00222
NM_004700.4(KCNQ4):c.1292+12G>A	rs200426006	0.00200
NM_004700.4(KCNQ4):c.1231C>T (p.Arg411Cys)	rs199809248	0.00141
NM_004700.4(KCNQ4):c.465A>C (p.Gly155=)	rs145129529	0.00081
NM_004700.4(KCNQ4):c.533-34G>A	rs567517894	0.00032
NM_004700.4(KCNQ4):c.1130+41G>A	rs141222961	0.00027
NM_004700.4(KCNQ4):c.438G>A (p.Glu146=)	rs144434662	0.00025
NM_004700.4(KCNQ4):c.735G>A (p.Gly245=)	rs147751558	0.00016
NM_004700.4(KCNQ4):c.1668C>T (p.Tyr556=)	rs140945833	0.00010
NM_004700.4(KCNQ4):c.176C>T (p.Pro59Leu)	rs775420649	0.00009
NM_004700.4(KCNQ4):c.2028C>T (p.Asp676=)	rs552843990	0.00009
NM_004700.4(KCNQ4):c.222G>A (p.Ser74=)	rs200001289	0.00006
NC_000001.11:g.40783732C>G	rs56048573
NM_004700.4(KCNQ4):c.1041+177C>A	rs79552281
NM_004700.4(KCNQ4):c.149G>A (p.Ser50Asn)	rs1553165192
NM_004700.4(KCNQ4):c.1514-226_1514-225del	rs3831140
NM_004700.4(KCNQ4):c.1614-208del	rs147459653
NM_004700.4(KCNQ4):c.191_202dup (p.62_63GS[5])	rs781081834
NM_004700.4(KCNQ4):c.405+120_405+166del	rs757160661
NM_004700.4(KCNQ4):c.822C>A (p.Leu274=)	rs1158481632

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