ClinVar Miner

List of variants in gene KCNQ4 studied for Nonsyndromic genetic hearing loss

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.720C>G (p.Thr240=)	rs752131356
NM_004700.4(KCNQ4):c.803CCT[1] (p.Ser269del)	rs797044966
NM_004700.4(KCNQ4):c.825G>C (p.Trp275Cys)	rs956666801
NM_004700.4(KCNQ4):c.853G>A (p.Gly285Ser)	rs28937588

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