List of variants in gene LGI1 reported as benign for 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005097.4(LGI1):c.657T>C (p.Phe219=)	rs1111820	0.97657
NM_005097.4(LGI1):c.674-18T>C	rs1108877	0.21834
NM_005097.4(LGI1):c.216-55T>C	rs143132529	0.00666
NM_005097.4(LGI1):c.345A>G (p.Pro115=)	rs151104648	0.00113
NM_005097.4(LGI1):c.1A>G (p.Met1Val)	rs202204627	0.00080
NM_005097.4(LGI1):c.600C>T (p.Cys200=)	rs148862146	0.00075
NM_005097.4(LGI1):c.1062T>G (p.Ala354=)	rs768151875	0.00016
NM_005097.4(LGI1):c.216-13del
NM_005097.4(LGI1):c.287+19A>G
NM_005097.4(LGI1):c.432-5dup	rs61662431
NM_005097.4(LGI1):c.432-6_432-5dup	rs61662431

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