ClinVar Miner

List of variants studied for autosomal recessive nonsyndromic hearing loss 86 by OMIM

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_001199107.2(TBC1D24):c.208G>T (p.Asp70Tyr) rs587777147
NM_001199107.2(TBC1D24):c.878G>C (p.Arg293Pro) rs199700840

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