ClinVar Miner

List of variants in gene COCH studied for autosomal dominant nonsyndromic hearing loss 9

Included ClinVar conditions (1):
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Gene type:
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Total variants: 17
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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

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