ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported as likely benign for Familial hemiplegic migraine

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Total variants: 17
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HGVS dbSNP
NM_006920.6(SCN1A):c.*1025T>C rs10497275
NM_006920.6(SCN1A):c.*1031A>T rs114522414
NM_006920.6(SCN1A):c.*1224G>A rs77088538
NM_006920.6(SCN1A):c.*1653C>T rs79971813
NM_006920.6(SCN1A):c.*1693A>G rs7591522
NM_006920.6(SCN1A):c.*172dup rs113696479
NM_006920.6(SCN1A):c.*1864T>A rs150155252
NM_006920.6(SCN1A):c.*1952T>C rs184794128
NM_006920.6(SCN1A):c.*1961C>T rs7577411
NM_006920.6(SCN1A):c.*588A>G rs539073575
NM_006920.6(SCN1A):c.3488C>G (p.Thr1163Ser) rs121918799
NM_006920.6(SCN1A):c.3690T>C (p.Tyr1230=) rs36031496
NM_006920.6(SCN1A):c.4518A>G (p.Lys1506=) rs374087499
NM_006920.6(SCN1A):c.4912C>T (p.Leu1638=) rs148546224
NM_006920.6(SCN1A):c.5385G>A (p.Glu1795=) rs140237315
NM_006920.6(SCN1A):c.5749C>G (p.Arg1917Gly) rs121917956
NM_006920.6(SCN1A):c.5831T>C (p.Ile1944Thr) rs35735053

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