List of variants reported as likely benign for Non-acquired combined pituitary hormone deficiency with spine abnormalities

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_178138.6(LHX3):c.454+3C>T	rs34356735	0.01324
NM_178138.6(LHX3):c.108G>A (p.Gln36=)	rs33998096	0.01071
NM_178138.6(LHX3):c.*747C>G	rs146752425	0.00653
NM_178138.6(LHX3):c.252-4G>T	rs372058376	0.00165
NM_178138.6(LHX3):c.*791G>A	rs12237402	0.00163
NM_178138.6(LHX3):c.920G>C (p.Arg307Pro)	rs182345541	0.00073
NM_178138.6(LHX3):c.79+1814G>T	rs569646536	0.00064
NM_178138.6(LHX3):c.964G>A (p.Ala322Thr)	rs201356862	0.00035
NM_178138.6(LHX3):c.534C>T (p.Thr178=)	rs564712080	0.00018
NM_178138.6(LHX3):c.87G>A (p.Pro29=)	rs183980824	0.00007
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.582G>C (p.Thr194=)	rs759590430
NM_178138.6(LHX3):c.79+1813G>C	rs886063706

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