List of variants in gene 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_018723.4(RBFOX1):c.-64+166491C>A	rs7187508	0.62707
NM_018723.4(RBFOX1):c.931-19A>G	rs2302213	0.10758
NM_018723.4(RBFOX1):c.126G>A (p.Thr42=)	rs17143930	0.03708
NM_018723.4(RBFOX1):c.137C>A (p.Pro46His)	rs113298071	0.00341
NM_018723.4(RBFOX1):c.96C>G (p.Pro32=)	rs143695164	0.00052
NM_018723.4(RBFOX1):c.270+10C>G	rs113881725	0.00051
NM_018723.4(RBFOX1):c.264C>T (p.Thr88=)	rs202136920	0.00038
NM_018723.4(RBFOX1):c.144C>T (p.Pro48=)	rs61742359	0.00027
NM_018723.4(RBFOX1):c.70C>T (p.Pro24Ser)	rs148751394	0.00026
NM_145893.3(RBFOX1):c.57G>A (p.Pro19=)	rs147261087	0.00016
NM_018723.4(RBFOX1):c.708G>A (p.Glu236=)	rs368113568	0.00009
NM_018723.4(RBFOX1):c.28-11del
NM_018723.4(RBFOX1):c.758-4G>T	rs112339093
NM_018723.4(RBFOX1):c.758-5C>T	rs368263619
NM_018723.4(RBFOX1):c.879G>A (p.Pro293=)	rs200006523
NM_018723.4(RBFOX1):c.879G>C (p.Pro293=)	rs200006523

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