ClinVar Miner

List of variants reported as benign for Epilepsy, lateral temporal lobe, autosomal dominant

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Total variants: 4
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HGVS dbSNP
NM_005097.4(LGI1):c.1A>G (p.Met1Val) rs202204627
NM_005097.4(LGI1):c.216-55T>C rs143132529
NM_005097.4(LGI1):c.345A>G (p.Pro115=) rs151104648
NM_005097.4(LGI1):c.600C>T (p.Cys200=) rs148862146

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