ClinVar Miner

List of variants reported as benign for Brugada syndrome 4

Included ClinVar conditions (1):
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_201596.3(CACNB2):c.*10G>T rs4747352 0.76187
NM_201596.3(CACNB2):c.670+2843T>C rs4748477 0.41677
NM_201596.3(CACNB2):c.1701C>T (p.Tyr567=) rs2228645 0.19212
NM_201596.3(CACNB2):c.1054+7C>T rs4314963 0.19120
NM_201596.3(CACNB2):c.1965T>G (p.Asp655Glu) rs58225473 0.14908
NM_201596.3(CACNB2):c.1518C>T (p.Arg506=) rs34813638 0.01090
NM_201596.3(CACNB2):c.1785C>T (p.His595=) rs61733967 0.00879
NM_201596.3(CACNB2):c.993G>A (p.Ser331=) rs76956014 0.00852
NM_201596.3(CACNB2):c.1794T>C (p.Ser598=) rs34503140 0.00787
NM_201596.3(CACNB2):c.1206+6T>C rs147857449 0.00575
NM_201596.3(CACNB2):c.214-61251C>A rs117558767 0.00414
NM_201596.3(CACNB2):c.1488+13_1488+33dup rs757040188 0.00361
NM_201596.3(CACNB2):c.873G>A (p.Leu291=) rs138423466 0.00355
NM_201596.3(CACNB2):c.915T>C (p.Phe305=) rs149586418 0.00282
NM_201596.3(CACNB2):c.354G>A (p.Ala118=) rs182163363 0.00107
NM_201596.3(CACNB2):c.1560T>C (p.Pro520=) rs150280879 0.00099
NM_201596.3(CACNB2):c.1293G>A (p.Gln431=) rs148414498 0.00093
NM_201596.3(CACNB2):c.641G>C (p.Ser214Thr) rs149253719 0.00078
NM_201596.3(CACNB2):c.1054+18G>A rs192538011 0.00039
NM_201596.3(CACNB2):c.1650C>T (p.Ser550=) rs149330185 0.00032
NM_201596.3(CACNB2):c.1488+9A>G rs368473992 0.00026
NM_201596.3(CACNB2):c.380C>T (p.Ala127Val) rs200367454 0.00022
NM_201596.3(CACNB2):c.1696G>A (p.Ala566Thr) rs202218948 0.00014
NM_201596.3(CACNB2):c.671-18T>C rs551760338 0.00011
NM_201596.3(CACNB2):c.1303-4G>A rs765944934 0.00006
NM_201596.3(CACNB2):c.426C>T (p.Phe142=) rs564275776 0.00002
NM_201596.3(CACNB2):c.944+20G>A rs760513979 0.00001
NM_201596.3(CACNB2):c.*35del rs34022725
NM_201596.3(CACNB2):c.120+379A>G
NM_201596.3(CACNB2):c.1521C>A (p.Ser507=) rs143060134
NM_201596.3(CACNB2):c.1521C>T (p.Ser507=) rs143060134
NM_201596.3(CACNB2):c.1670C>T (p.Ser557Leu) rs137886839
NM_201596.3(CACNB2):c.1816C>G (p.Arg606Gly) rs61733968
NM_201596.3(CACNB2):c.457-17T>G rs4485000
NM_201596.3(CACNB2):c.622T>C (p.Leu208=) rs538160664
NM_201596.3(CACNB2):c.711T>C (p.Asn237=) rs570005089
NM_201596.3(CACNB2):c.944+12A>T rs144304963

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