ClinVar Miner

List of variants studied for Hearing loss, autosomal dominant 73 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_001145026.2(PTPRQ):c.3G>A (p.Met1Ile) rs916582229 0.00001
NM_001145026.2(PTPRQ):c.5606A>G (p.Gln1869Arg) rs1275679740

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