ClinVar Miner

List of variants in gene PTPRQ reported as uncertain significance for Hearing impairment

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001145026.2(PTPRQ):c.1015A>G (p.Arg339Gly) rs1245108213 0.00005
NM_001145026.2(PTPRQ):c.2546C>T (p.Thr849Met) rs974503422 0.00005
NM_001145026.2(PTPRQ):c.1133C>A (p.Thr378Asn) rs2120546591
NM_001145026.2(PTPRQ):c.6883G>A (p.Glu2295Lys) rs2121305975

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