ClinVar Miner

List of variants in gene CACNA1H reported as benign for Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV

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Total variants: 14
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HGVS dbSNP
NM_021098.3(CACNA1H):c.1120-8C>T rs59091981
NM_021098.3(CACNA1H):c.2544C>T (p.Gly848=) rs28365123
NM_021098.3(CACNA1H):c.2907+9C>T rs200631961
NM_021098.3(CACNA1H):c.3175G>T (p.Ala1059Ser) rs41292285
NM_021098.3(CACNA1H):c.3738G>A (p.Ser1246=) rs58812334
NM_021098.3(CACNA1H):c.390C>T (p.Ser130=) rs59794024
NM_021098.3(CACNA1H):c.4555G>A (p.Val1519Ile) rs1462779871
NM_021098.3(CACNA1H):c.4817C>T (p.Thr1606Met) rs59286323
NM_021098.3(CACNA1H):c.546-10C>T rs35509671
NM_021098.3(CACNA1H):c.5897C>T (p.Ala1966Val) rs72552054
NM_021098.3(CACNA1H):c.5921A>G (p.Glu1974Gly) rs3751886
NM_021098.3(CACNA1H):c.6324C>T (p.Ala2108=) rs57670193
NM_021098.3(CACNA1H):c.993C>A (p.Gly331=) rs770821118
NM_021098.3(CACNA1H):c.994G>A (p.Ala332Thr) rs59650398

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