ClinVar Miner

List of variants in gene COCH reported as uncertain significance for auditory system disorder

Included ClinVar conditions (322):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
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.*58A>G rs886050444 0.00001
NM_004086.3(COCH):c.*377T>C rs1895934392
NM_004086.3(COCH):c.*568A>C rs978000615

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