List of variants reported as pathogenic for Seizures, benign familial infantile, 2 by OMIM

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_145239.3(PRRT2):c.291del (p.Asn98fs)	rs730882073
NM_145239.3(PRRT2):c.629del (p.Pro210fs)	rs730882067
NM_145239.3(PRRT2):c.649dup (p.Arg217fs)
NM_145239.3(PRRT2):c.650del (p.Arg217fs)	rs730882124
NM_145239.3(PRRT2):c.748C>T (p.Gln250Ter)	rs397514579
NM_145239.3(PRRT2):c.879+5G>A	rs1596893185

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