ClinVar Miner

List of variants in gene LHX3 reported as benign for combined pituitary hormone deficiencies, genetic form

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_178138.6(LHX3):c.79+2007T>C rs2274115 0.71807
NM_178138.6(LHX3):c.776-90C>T rs7860634 0.55589
NM_178138.6(LHX3):c.79+1975G>A rs2274116 0.23265
NM_178138.6(LHX3):c.454+64C>T rs2274114 0.21362
NM_178138.6(LHX3):c.251+30G>A rs75290716 0.05544
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.*825C>A rs3739470 0.00510
NM_178138.6(LHX3):c.*185T>A rs144976921 0.00202
NM_178138.6(LHX3):c.79+1935C>G rs769912904 0.00016
NM_178138.6(LHX3):c.251+148T>C rs1886296

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