List of variants reported as uncertain significance for Developmental and epileptic encephalopathy, 1 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_139058.3(ARX):c.1128C>G (p.Phe376Leu)	rs2048683301
NM_139058.3(ARX):c.1522G>A (p.Val508Met)	rs2048670414
NM_139058.3(ARX):c.1546G>T (p.Ala516Ser)	rs747042039
NM_139058.3(ARX):c.1684T>C (p.Cys562Arg)	rs2048668859
NM_139058.3(ARX):c.451_465del (p.Ala151_Ala155del)	rs757588621
NM_139058.3(ARX):c.946G>A (p.Gly316Ser)	rs2048708756

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