List of variants reported as pathogenic for neurodevelopmental disorder with severe motor impairment and absent language by OMIM

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_138615.3(DHX30):c.1478G>A (p.Arg493His)	rs1057519436
NM_138615.3(DHX30):c.1685A>G (p.His562Arg)	rs1060499733
NM_138615.3(DHX30):c.2342G>A (p.Gly781Asp)	rs1553706775
NM_138615.3(DHX30):c.2344C>T (p.Arg782Trp)	rs753242774
NM_138615.3(DHX30):c.2353C>T (p.Arg785Cys)	rs1085307451
NM_138615.3(DHX30):c.2354G>A (p.Arg785His)	rs1553706799
NM_138615.3(DHX30):c.2389C>T (p.Arg797Ter)

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