ClinVar Miner

List of variants in gene GNRHR 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: 74
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HGVS dbSNP gnomAD frequency
NM_000406.3(GNRHR):c.*2196G>A rs145112872 0.00495
NM_000406.3(GNRHR):c.*495T>C rs115861964 0.00467
NM_000406.3(GNRHR):c.*2802T>C rs79040488 0.00275
NM_000406.2(GNRHR):c.-1636T>C rs750872049 0.00223
NM_000406.3(GNRHR):c.*1301A>G rs190775695 0.00160
NM_000406.2(GNRHR):c.-107C>T rs184491810 0.00156
NM_000406.3(GNRHR):c.*3011T>C rs561253321 0.00149
NM_000406.3(GNRHR):c.*1892C>A rs183815234 0.00144
NM_000406.3(GNRHR):c.*2919A>G rs149178613 0.00112
NM_000406.3(GNRHR):c.*1654C>T rs184206874 0.00100
NM_000406.3(GNRHR):c.436C>T (p.Pro146Ser) rs144900788 0.00076
NM_000406.3(GNRHR):c.576T>C (p.Val192=) rs147822774 0.00050
NM_000406.2(GNRHR):c.-1563T>C rs560053680 0.00042
NM_000406.3(GNRHR):c.-8G>A rs199976279 0.00036
NM_000406.3(GNRHR):c.*1347A>G rs765394872 0.00018
NM_000406.3(GNRHR):c.*2588C>T rs377155481 0.00016
NM_000406.3(GNRHR):c.*912C>T rs963694391 0.00015
NM_000406.2(GNRHR):c.-1239T>A rs879487074 0.00014
NM_000406.3(GNRHR):c.*193A>G rs529064600 0.00013
NM_000406.3(GNRHR):c.719G>A (p.Arg240Gln) rs182531866 0.00012
NM_000406.3(GNRHR):c.281T>C (p.Val94Ala) rs367560743 0.00011
NM_000406.3(GNRHR):c.*1193C>T rs886059561 0.00009
NM_000406.3(GNRHR):c.*806G>C rs113838900 0.00008
NM_000406.2(GNRHR):c.-1702A>G rs560099007 0.00007
NM_000406.3(GNRHR):c.666C>T (p.Ile222=) rs377457276 0.00007
NM_000406.3(GNRHR):c.*1948C>T rs886059558 0.00006
NM_000406.3(GNRHR):c.*1275G>A rs763058779 0.00005
NM_000406.3(GNRHR):c.*1797A>G rs989136388 0.00005
NM_000406.3(GNRHR):c.648C>T (p.Phe216=) rs144451862 0.00005
NM_000406.3(GNRHR):c.*2248T>C rs576475427 0.00004
NM_000406.3(GNRHR):c.*3076T>C rs886059554 0.00004
NM_000406.2(GNRHR):c.-980G>A rs886059576 0.00003
NM_000406.3(GNRHR):c.*696A>T rs1422742508 0.00003
NM_000406.3(GNRHR):c.743-9A>G rs886059567 0.00003
NM_000406.2(GNRHR):c.-1059G>C rs569550069 0.00002
NM_000406.3(GNRHR):c.*2165A>G rs886059555 0.00002
NM_000406.2(GNRHR):c.-1251T>C rs995685917 0.00001
NM_000406.2(GNRHR):c.-1741G>T rs886059579 0.00001
NM_000406.2(GNRHR):c.-721A>G rs886059571 0.00001
NM_000406.2(GNRHR):c.-922A>G rs886059573 0.00001
NM_000406.3(GNRHR):c.*1532C>A rs528286579 0.00001
NM_000406.3(GNRHR):c.*2748C>T rs1314834107 0.00001
NM_000406.3(GNRHR):c.*622T>C rs1029319746 0.00001
NM_000406.3(GNRHR):c.*662T>C rs535382437 0.00001
NM_000406.3(GNRHR):c.*668G>A rs1476710655 0.00001
NM_000406.3(GNRHR):c.*928C>A rs1011196434 0.00001
NM_000406.3(GNRHR):c.399G>A (p.Val133=) rs1245052683 0.00001
NM_000406.2(GNRHR):c.-1319C>T rs886059578
NM_000406.2(GNRHR):c.-1434A>T rs542889610
NM_000406.2(GNRHR):c.-1464G>A rs1731958615
NM_000406.2(GNRHR):c.-1701A>C rs546717493
NM_000406.2(GNRHR):c.-576G>T rs886059569
NM_000406.2(GNRHR):c.-699T>C rs1731942957
NM_000406.2(GNRHR):c.-877C>A rs886059572
NM_000406.2(GNRHR):c.-927C>T rs886059574
NM_000406.2(GNRHR):c.-962G>A rs886059575
NM_000406.3(GNRHR):c.*1144A>G rs886059562
NM_000406.3(GNRHR):c.*1248A>C rs886059560
NM_000406.3(GNRHR):c.*1302G>C rs555225443
NM_000406.3(GNRHR):c.*1984T>C rs886059557
NM_000406.3(GNRHR):c.*2244T>C rs1231172432
NM_000406.3(GNRHR):c.*2328A>T rs781061386
NM_000406.3(GNRHR):c.*2772A>G rs1731573809
NM_000406.3(GNRHR):c.*349A>C rs886059565
NM_000406.3(GNRHR):c.*466T>G rs1731627479
NM_000406.3(GNRHR):c.*474T>C rs1731627299
NM_000406.3(GNRHR):c.*730T>C rs566465436
NM_000406.3(GNRHR):c.*819A>T rs886059564
NM_000406.3(GNRHR):c.*832T>C rs886059563
NM_000406.3(GNRHR):c.12T>G (p.Ser4Arg) rs764414922
NM_000406.3(GNRHR):c.215A>G (p.Lys72Arg) rs1731924174
NM_000406.3(GNRHR):c.465C>T (p.Val155=) rs773986790
NM_000406.3(GNRHR):c.773T>C (p.Ile258Thr) rs886059566
NM_000406.3(GNRHR):c.94A>G (p.Thr32Ala) rs515726219

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