List of variants reported as likely benign for Seizures, benign familial neonatal, 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004519.4(KCNQ3):c.1059C>T (p.Ser353=)	rs35413925	0.01009
NM_004519.4(KCNQ3):c.1551C>T (p.Ala517=)	rs35538317	0.00761
NM_004519.4(KCNQ3):c.2306C>A (p.Pro769His)	rs114095081	0.00702
NM_004519.4(KCNQ3):c.2168G>A (p.Gly723Glu)	rs142149782	0.00334
NM_004519.4(KCNQ3):c.1236-16C>T	rs201168632	0.00301
NM_004519.4(KCNQ3):c.1568+8C>T	rs370337209	0.00002

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