List of variants in gene COCH studied for nonsyndromic genetic hearing loss

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_004086.3(COCH):c.*27A>T	rs13122	0.24742
NM_004086.3(COCH):c.*407C>T	rs7152503	0.02116
NM_004086.3(COCH):c.*814G>A	rs543797568	0.00198
NM_004086.3(COCH):c.*625T>C	rs143467211	0.00149
NM_004086.3(COCH):c.*245G>A	rs45624239	0.00127
NM_004086.3(COCH):c.*339T>C	rs187461561	0.00113
NM_004086.3(COCH):c.*237G>C	rs190142757	0.00035
NM_004086.3(COCH):c.*432T>C	rs867385285	0.00013
NM_004086.3(COCH):c.*342A>T	rs913851990	0.00006
NM_004086.3(COCH):c.*358G>A	rs774390888	0.00005
NM_004086.3(COCH):c.-10A>G	rs200113981	0.00002
NM_004086.3(COCH):c.*275C>T	rs886050445	0.00001
NM_004086.3(COCH):c.*39G>T	rs555882283	0.00001
NM_004086.3(COCH):c.*58A>G	rs886050444	0.00001
NM_004086.3(COCH):c.*377T>C	rs1895934392
NM_004086.3(COCH):c.*568A>C	rs978000615
NM_004086.3(COCH):c.*612G>T	rs541766600
NM_004086.3(COCH):c.7G>C (p.Ala3Pro)

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