List of variants reported as uncertain significance for epilepsy by Knight Diagnostic Laboratories, Oregon Health and Sciences University

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001367561.1(DOCK7):c.3797G>A (p.Arg1266Gln)	rs138914992	0.00019
NM_001365536.1(SCN9A):c.4820C>T (p.Thr1607Ile)	rs200470541	0.00012
NM_001191061.2(SLC25A22):c.562A>G (p.Lys188Glu)	rs767949941	0.00004
NM_005458.8(GABBR2):c.56C>T (p.Pro19Leu)	rs1054346747	0.00004
NM_000100.4(CSTB):c.158A>G (p.Tyr53Cys)	rs762082236	0.00002
NM_001367561.1(DOCK7):c.38+6T>C	rs1029588198	0.00002
NM_001365999.1(SZT2):c.2599G>A (p.Val867Ile)	rs768015377	0.00001
NM_007254.4(PNKP):c.1360C>G (p.Leu454Val)	rs200611702
NM_020708.5(SLC12A5):c.2452C>G (p.Pro818Ala)	rs201268862

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