ClinVar Miner

List of variants studied for 46,XY sex reversal 11

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_032656.4(DHX37):c.1294-38T>C rs10773130 0.94520
NM_032656.4(DHX37):c.2579-7T>C rs4606565 0.57988
NM_032656.4(DHX37):c.2605A>G (p.Ser869Gly) rs4516060 0.57836
NM_032656.4(DHX37):c.3242G>A (p.Arg1081Gln) rs4447263 0.56855
NM_032656.4(DHX37):c.2695+12T>C rs12367953 0.56686
NM_032656.4(DHX37):c.2793A>G (p.Ala931=) rs4429156 0.56645
NM_032656.4(DHX37):c.2598G>A (p.Glu866=) rs4258464 0.56360
NM_032656.4(DHX37):c.2869-38G>A rs10773125 0.50743
NM_032656.4(DHX37):c.2046-6A>G rs4765007 0.50353
NM_032656.4(DHX37):c.738+13G>A rs4072887 0.39088
NM_032656.4(DHX37):c.288G>A (p.Met96Ile) rs11558556 0.36027
NM_032656.4(DHX37):c.2578+17T>G rs11831506 0.26617
NM_032656.4(DHX37):c.2696-26G>A rs6488959 0.26288
NM_032656.4(DHX37):c.3195C>T (p.Ala1065=) rs4078216 0.20190
NM_032656.4(DHX37):c.985G>A (p.Val329Ile) rs112262509 0.00039
NM_032656.4(DHX37):c.451C>T (p.Arg151Trp) rs577400960 0.00005
NM_032656.4(DHX37):c.1460G>A (p.Arg487His) rs779613772 0.00004
NM_032656.4(DHX37):c.2956G>A (p.Val986Met) rs111456585 0.00003
NM_032656.4(DHX37):c.1829C>T (p.Pro610Leu) rs775249132 0.00001
NM_032656.4(DHX37):c.923G>A (p.Arg308Gln) rs1384892917 0.00001
NM_032656.4(DHX37):c.1000C>T (p.Arg334Trp)
NM_032656.4(DHX37):c.1784C>T (p.Ser595Phe) rs1954346640
NM_032656.4(DHX37):c.1877C>T (p.Ser626Leu) rs2135945152
NM_032656.4(DHX37):c.2020C>T (p.Arg674Trp) rs1954336272
NM_032656.4(DHX37):c.2021G>A (p.Arg674Gln) rs1954336215
NM_032656.4(DHX37):c.2331A>G (p.Thr777=) rs10773127
NM_032656.4(DHX37):c.2776C>T (p.Arg926Ter)
NM_032656.4(DHX37):c.499_500inv (p.Glu167Ser)
NM_032656.4(DHX37):c.911C>T (p.Thr304Met) rs1954619788
NM_032656.4(DHX37):c.994C>G (p.Gln332Glu)

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