List of variants reported as likely benign for electroclinical syndrome by Genome Diagnostics Laboratory, University Medical Center Utrecht

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_015192.4(PLCB1):c.2413+9C>T	rs138442805	0.00934
NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=)	rs61753382	0.00763
NM_004519.4(KCNQ3):c.2306C>A (p.Pro769His)	rs114095081	0.00702
NM_015192.4(PLCB1):c.1469A>G (p.Tyr490Cys)	rs45608240	0.00391
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser)	rs77029288	0.00068
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=)	rs77705198	0.00059

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