List of variants reported as uncertain significance for developmental and epileptic encephalopathy, 64 by New York Genome Center

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_015178.3(RHOBTB2):c.1039G>A (p.Val347Met)	rs762216794	0.00003
NM_015178.3(RHOBTB2):c.1621G>A (p.Val541Met)	rs1328047091	0.00001
NM_015178.3(RHOBTB2):c.2038C>T (p.Arg680Trp)	rs767630251	0.00001
NM_015178.3(RHOBTB2):c.1488del (p.Gly497fs)	rs1376454917
NM_015178.3(RHOBTB2):c.1541A>G (p.His514Arg)	rs2128805194
NM_015178.3(RHOBTB2):c.978C>A (p.His326Gln)	rs559073741

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