ClinVar Miner

List of variants in gene LHX3 reported as benign for not provided

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_178138.6(LHX3):c.79+2007T>C rs2274115 0.71807
NM_178138.6(LHX3):c.79+1509G>C rs3758197 0.66885
NC_000009.12:g.136205359T>C rs11103378 0.62300
NM_178138.6(LHX3):c.80-80A>G rs4842131 0.56460
NM_178138.6(LHX3):c.776-128A>C rs7850466 0.55658
NM_178138.6(LHX3):c.776-129T>G rs7847312 0.55647
NM_178138.6(LHX3):c.776-90C>T rs7860634 0.55589
NC_000009.12:g.136205289A>G rs11103377 0.46306
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.-40A>C rs10858245 0.19945
NM_178138.6(LHX3):c.251+30G>A rs75290716 0.05544
NM_178138.6(LHX3):c.251+233G>C rs60275143 0.04809
NM_178138.6(LHX3):c.455-97G>C rs553463579 0.02288
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.252-4G>T rs372058376 0.00165
NM_178138.6(LHX3):c.705C>G (p.Arg235=) rs138595537 0.00073
NM_178138.6(LHX3):c.964G>A (p.Ala322Thr) rs201356862 0.00035
NM_178138.6(LHX3):c.607-16C>G rs200569650 0.00032
NM_178138.6(LHX3):c.79+1935C>G rs769912904 0.00016
NM_178138.6(LHX3):c.198C>G (p.Ala66=) rs190916587 0.00010
NM_178138.6(LHX3):c.*104del rs146678449
NM_178138.6(LHX3):c.251+148T>C rs1886296
NM_178138.6(LHX3):c.251+15del rs540380272
NM_178138.6(LHX3):c.252-71T>G rs1924521
NM_178138.6(LHX3):c.775+25_775+26dup rs3215774
NM_178138.6(LHX3):c.775+25dup rs3215774
NM_178138.6(LHX3):c.775+30_775+31insC rs201352295
NM_178138.6(LHX3):c.776-161G>A rs12379555
NM_178138.6(LHX3):c.79+2004G>A
NM_178138.6(LHX3):c.915G>A (p.Gln305=) rs548140963

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