List of variants in gene KCNQ4 reported as pathogenic for obsolete rare genetic deafness

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.827G>C (p.Trp276Ser)	rs80358277	0.00001
NM_004700.4(KCNQ4):c.459del (p.Ala154fs)	rs727504635
NM_004700.4(KCNQ4):c.853G>A (p.Gly285Ser)	rs28937588

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