List of variants reported as pathogenic for febrile seizures, familial by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.6901C>T (p.Gln2301Ter)	rs121909762	0.00004
NM_032119.4(ADGRV1):c.17062C>T (p.Arg5688Ter)	rs747622607	0.00002
NM_032119.4(ADGRV1):c.2398C>T (p.Arg800Ter)	rs373780305	0.00001
NM_001165963.4(SCN1A):c.1354A>T (p.Lys452Ter)	rs1553546668
NM_001165963.4(SCN1A):c.141del (p.Asn47fs)	rs796053076
NM_001165963.4(SCN1A):c.1837C>T (p.Arg613Ter)	rs398123585
NM_001165963.4(SCN1A):c.2792G>A (p.Arg931His)	rs794726718
NM_001165963.4(SCN1A):c.3733C>T (p.Arg1245Ter)	rs727504136
NM_001165963.4(SCN1A):c.4547C>A (p.Ser1516Ter)	rs139300715
NM_001165963.4(SCN1A):c.4934G>A (p.Arg1645Gln)	rs121917976
NM_001165963.4(SCN1A):c.5347G>A (p.Ala1783Thr)	rs121917980
NM_001165963.4(SCN1A):c.5674C>T (p.Arg1892Ter)	rs794726739
NM_001165963.4(SCN1A):c.664C>T (p.Arg222Ter)	rs121918624
NM_001165963.4(SCN1A):c.677C>T (p.Thr226Met)	rs121917984
NM_001165963.4(SCN1A):c.839G>A (p.Trp280Ter)	rs1698593264

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