List of variants reported as benign for Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV by Fulgent Genetics, Fulgent Genetics

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_021098.3(CACNA1H):c.1664C>T (p.Ala555Val)	rs9924241	0.01528
NM_021098.3(CACNA1H):c.3738G>A (p.Ser1246=)	rs58812334	0.01201
NM_021098.3(CACNA1H):c.2881C>T (p.Leu961=)	rs58615599	0.00607
NM_021098.3(CACNA1H):c.5324-4G>A	rs57687113	0.00558
NM_021098.3(CACNA1H):c.1381C>T (p.Leu461=)	rs57112868	0.00508
NM_021098.3(CACNA1H):c.1359T>C (p.Pro453=)	rs60720455	0.00507
NM_021098.3(CACNA1H):c.4932G>A (p.Ser1644=)	rs58764017	0.00488
NM_021098.3(CACNA1H):c.1479T>C (p.Ser493=)	rs60415676	0.00425
NM_021098.3(CACNA1H):c.4038+12C>T	rs370831984	0.00414
NM_021098.3(CACNA1H):c.819C>T (p.Thr273=)	rs72552033	0.00150
NM_021098.3(CACNA1H):c.5173+18C>T	rs373269618	0.00089
NM_021098.3(CACNA1H):c.1824G>A (p.Leu608=)	rs57260464	0.00083
NM_021098.3(CACNA1H):c.3970-6C>T	rs200403676	0.00053
NM_021098.3(CACNA1H):c.3300C>T (p.Leu1100=)	rs568667163	0.00009
NM_021098.3(CACNA1H):c.299+15C>G	rs553478910
NM_021098.3(CACNA1H):c.4038+15G>T	rs375169106

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