ClinVar Miner

List of variants in gene OTX2 reported as uncertain significance for congenital hypogonadotropic hypogonadism

Included ClinVar conditions (68):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_021728.4(OTX2):c.*667A>C rs184421963 0.00024
NM_021728.4(OTX2):c.273+11T>C rs371958059 0.00021
NM_021728.4(OTX2):c.425C>G (p.Pro142Arg) rs199761861 0.00016
NM_021728.4(OTX2):c.*764G>A rs775857186 0.00014
NM_021728.4(OTX2):c.-119-65G>T rs886050561 0.00010
NM_021728.4(OTX2):c.406A>G (p.Ser136Gly) rs770291855 0.00004
NM_021728.4(OTX2):c.*219G>A rs886050559 0.00003
NM_021728.4(OTX2):c.*647A>G rs886050557 0.00003
NM_021728.4(OTX2):c.270G>T (p.Val90=) rs747916036 0.00003
NM_021728.4(OTX2):c.713A>T (p.His238Leu) rs144449264 0.00003
NM_021728.4(OTX2):c.*1018T>C rs1594950988 0.00001
NM_021728.4(OTX2):c.*147G>T rs1478094910 0.00001
NM_021728.4(OTX2):c.*543A>G rs948990605 0.00001
NM_021728.4(OTX2):c.*648C>A rs886050556 0.00001
NM_021728.4(OTX2):c.*648C>G rs886050556
NM_021728.4(OTX2):c.*933C>T rs886050555
NM_021728.4(OTX2):c.*993G>C rs1891845026
NM_021728.4(OTX2):c.380G>A (p.Arg127Gln) rs199799627
NM_021728.4(OTX2):c.380G>C (p.Arg127Pro) rs199799627
NM_021728.4(OTX2):c.380G>T (p.Arg127Leu) rs199799627
NM_021728.4(OTX2):c.444G>A (p.Pro148=) rs147896150
NM_021728.4(OTX2):c.464C>G (p.Ala155Gly) rs200171280
NM_021728.4(OTX2):c.730G>A (p.Ala244Thr) rs1594952158
NM_021728.4(OTX2):c.96G>T (p.Pro32=) rs1892046623

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