ClinVar Miner

List of variants reported as benign for congenital hypogonadotropic hypogonadism by Natera, Inc.

Included ClinVar conditions (69):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_006261.5(PROP1):c.59A>G (p.Asn20Ser) rs7445271 0.99974
NM_006261.5(PROP1):c.109+3G>A rs4072924 0.54780
NM_006261.5(PROP1):c.27T>C (p.Ala9=) rs1135320 0.40746
NM_178138.6(LHX3):c.79+1975G>A rs2274116 0.23265
NM_006261.5(PROP1):c.424G>A (p.Ala142Thr) rs1800197 0.22589
NM_006261.5(PROP1):c.109+435G>A rs73346254 0.06917
NM_006261.5(PROP1):c.174G>A (p.Pro58=) rs2233784 0.02188
NM_178138.6(LHX3):c.454+3C>T rs34356735 0.01349
NM_178138.6(LHX3):c.108G>A (p.Gln36=) rs33998096 0.01071
NM_178138.6(LHX3):c.79+1935C>G rs769912904 0.00016
NM_006261.5(PROP1):c.152G>C (p.Gly51Ala) rs2233783

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