List of variants in gene combination LOC126862279, RBFOX1 reported as benign for genetic generalized epilepsy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_018723.4(RBFOX1):c.1071+3G>A	rs79369633	0.01704
NM_018723.4(RBFOX1):c.1032C>T (p.His344=)	rs534312610	0.00006
NM_018723.4(RBFOX1):c.996-19A>C	rs200846246	0.00006

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