List of variants reported as likely pathogenic for electroclinical syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001127644.2(GABRA1):c.640C>T (p.Arg214Cys)	rs727503940
NM_001199107.2(TBC1D24):c.1360_1363dup (p.Pro455fs)	rs1292551263
NM_001330260.2(SCN8A):c.5606T>C (p.Met1869Thr)	rs1064794727
NM_139058.3(ARX):c.994C>G (p.Arg332Gly)	rs2147323593
NM_172107.4(KCNQ2):c.365C>T (p.Ser122Leu)	rs118192194
NM_172107.4(KCNQ2):c.380A>G (p.Tyr127Cys)	rs796052617

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