List of variants reported as pathogenic for epilepsy, X-linked 1, with variable learning disabilities and behavior disorders by OMIM

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006950.3(SYN1):c.1067G>A (p.Trp356Ter)	rs137852560
NM_006950.3(SYN1):c.1264C>T (p.Arg422Ter)	rs757027813
NM_006950.3(SYN1):c.1266del (p.Gln423fs)
NM_006950.3(SYN1):c.1406dup (p.Pro470fs)
NM_006950.3(SYN1):c.1444C>T (p.Gln482Ter)
NM_006950.3(SYN1):c.1648G>A (p.Ala550Thr)	rs397514680
NM_006950.3(SYN1):c.1663C>T (p.Gln555Ter)	rs397514679
NM_006950.3(SYN1):c.527+1G>T

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