List of variants reported as pathogenic for epilepsy by Center of Medical Genomics-TUH, Thammasat University

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.719C>T (p.Ala240Val)	rs1553567864
NM_001165963.4(SCN1A):c.955C>T (p.Gln319Ter)
NM_001184880.2(PCDH19):c.1019A>G (p.Asn340Ser)	rs796052839
NM_001271.4(CHD2):c.1719+1G>A

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