ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported as likely benign for Epilepsy

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Total variants: 17
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HGVS dbSNP
NM_001165963.1(SCN1A):c.*1025T>C rs10497275
NM_001165963.1(SCN1A):c.*1031A>T rs114522414
NM_001165963.1(SCN1A):c.*1224G>A rs77088538
NM_001165963.1(SCN1A):c.*1653C>T rs79971813
NM_001165963.1(SCN1A):c.*1693A>G rs7591522
NM_001165963.1(SCN1A):c.*172dupG rs113696479
NM_001165963.1(SCN1A):c.*1864T>A rs150155252
NM_001165963.1(SCN1A):c.*1952T>C rs184794128
NM_001165963.1(SCN1A):c.*1961C>T rs7577411
NM_001165963.1(SCN1A):c.*588A>G rs539073575
NM_001165963.1(SCN1A):c.4551A>G (p.Lys1517=) rs374087499
NM_001165963.1(SCN1A):c.4945C>T (p.Leu1649=) rs148546224
NM_001165963.1(SCN1A):c.5418G>A (p.Glu1806=) rs140237315
NM_001165963.1(SCN1A):c.5864T>C (p.Ile1955Thr) rs35735053
NM_006920.4(SCN1A):c.3488C>G (p.Thr1163Ser) rs121918799
NM_006920.4(SCN1A):c.3690T>C (p.Tyr1230=) rs36031496
NM_006920.4(SCN1A):c.5749C>G (p.Arg1917Gly) rs121917956

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