ClinVar Miner

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

Included ClinVar conditions (118):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_001292063.2(OTOG):c.3285G>A (p.Trp1095Ter)
NM_001292063.2(OTOG):c.540G>T (p.Gln180His)
NM_001292063.2(OTOG):c.7199del (p.Cys2400fs) rs1565127413

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