ClinVar Miner

List of variants in gene GNRH1 studied for reproductive system disorder

Included ClinVar conditions (663):
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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001083111.2(GNRH1):c.47G>C (p.Trp16Ser) rs6185 0.20281
NM_001083111.2(GNRH1):c.-2+388T>C rs17790824 0.04306
NM_001083111.2(GNRH1):c.183C>T (p.Phe61=) rs6186 0.01376
NM_001083111.2(GNRH1):c.-2+5A>C rs78322917 0.01139
NM_001083111.2(GNRH1):c.141G>C (p.Glu47Asp) rs35542850 0.00159
NM_001083111.2(GNRH1):c.-2+194C>A rs534899690 0.00037
NM_001083111.2(GNRH1):c.177A>G (p.Gln59=) rs368837931 0.00022
NM_001083111.2(GNRH1):c.-2+59G>T rs962938386 0.00014
NM_000825.3(GNRH1):c.-1316C>T rs912543990 0.00010
NM_001083111.2(GNRH1):c.-1-110A>G rs886062837 0.00004
NM_001083111.2(GNRH1):c.237+8A>C rs751932727 0.00004
NM_001083111.2(GNRH1):c.143T>G (p.Ile48Arg) rs201184458 0.00002
NM_000825.3(GNRH1):c.-984C>G rs566037144 0.00001
NM_001083111.2(GNRH1):c.-1-140G>A rs886062838 0.00001
NM_001083111.2(GNRH1):c.238-12T>C rs550878484 0.00001
NM_001083111.2(GNRH1):c.92G>A (p.Arg31His) rs1336171284 0.00001
NM_000825.3(GNRH1):c.-1198G>A rs1801818194
NM_000825.3(GNRH1):c.-1624G>A rs1045519607
NM_001083111.2(GNRH1):c.18dup (p.Leu7fs) rs587777758
NM_001083111.2(GNRH1):c.210T>A (p.Ser70=) rs1801773599

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