List of variants in gene LHX4 reported as uncertain significance for combined pituitary hormone deficiencies, genetic form

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_033343.4(LHX4):c.-121T>G	rs547988090	0.00019
NM_033343.4(LHX4):c.-134G>C	rs565557892	0.00017
NM_033343.4(LHX4):c.248+13G>A	rs375232367	0.00016
NM_033343.4(LHX4):c.146A>G (p.His49Arg)	rs368995644	0.00007
NM_033343.4(LHX4):c.-221G>A	rs532307461	0.00003
NM_033343.4(LHX4):c.378G>A (p.Thr126=)	rs751665904	0.00002
NM_033343.4(LHX4):c.-172A>G	rs376657735
NM_033343.4(LHX4):c.269C>G (p.Thr90Arg)	rs773975101
NM_033343.4(LHX4):c.359G>A (p.Cys120Tyr)	rs1553282666
NM_033343.4(LHX4):c.364C>T (p.Arg122Trp)
NM_033343.4(LHX4):c.37_39del (p.Val13del)
NM_033343.4(LHX4):c.451+15C>T	rs886045598
NM_033343.4(LHX4):c.451G>C (p.Asp151His)
NM_033343.4(LHX4):c.83C>T (p.Pro28Leu)	rs886045597
NM_033343.4(LHX4):c.90C>G (p.Cys30Trp)	rs147491286

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