ClinVar Miner

List of variants in gene LHX3 reported as likely benign for congenital hypogonadotropic hypogonadism

Included ClinVar conditions (68):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP gnomAD frequency
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.*747C>G rs146752425 0.00714
NM_178138.6(LHX3):c.*791G>A rs12237402 0.00091
NM_178138.6(LHX3):c.920G>C (p.Arg307Pro) rs182345541 0.00073
NM_178138.6(LHX3):c.964G>A (p.Ala322Thr) rs201356862 0.00035
NM_178138.6(LHX3):c.441C>T (p.Thr147=) rs200521449 0.00024
NM_178138.6(LHX3):c.534C>T (p.Thr178=) rs564712080 0.00018
NM_178138.6(LHX3):c.309G>T (p.Val103=) rs766945737 0.00008
NM_178138.6(LHX3):c.87G>A (p.Pro29=) rs183980824 0.00006
NM_178138.6(LHX3):c.919C>A (p.Arg307=) rs145867977 0.00006
NM_178138.6(LHX3):c.93C>T (p.Cys31=) rs558712702 0.00004
NM_178138.6(LHX3):c.555C>A (p.His185Gln) rs760626241 0.00003
NM_178138.6(LHX3):c.79+1814G>T rs569646536 0.00003
NM_178138.6(LHX3):c.79+1933G>C rs1391957672 0.00001
NM_178138.6(LHX3):c.582G>C (p.Thr194=) rs759590430

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