ClinVar Miner

List of variants in gene combination CACNB2, NSUN6 reported as likely benign for Brugada syndrome

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Total variants: 22
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HGVS dbSNP
NM_201596.3(CACNB2):c.*10G>T rs4747352
NM_201596.3(CACNB2):c.*1330_*1333dup rs33980121
NM_201596.3(CACNB2):c.*1665T>C rs80130376
NM_201596.3(CACNB2):c.*17T>C rs58830289
NM_201596.3(CACNB2):c.*1965C>T rs10828872
NM_201596.3(CACNB2):c.*2016T>C rs7079776
NM_201596.3(CACNB2):c.*463_*466dup rs373389018
NM_201596.3(CACNB2):c.*516_*519dup rs201149401
NM_201596.3(CACNB2):c.*52_*55dup rs199830080
NM_201596.3(CACNB2):c.*571_*573dup rs35402411
NM_201596.3(CACNB2):c.*600_*601TA[4] rs72366492
NM_201596.3(CACNB2):c.*608T>A rs4748484
NM_201596.3(CACNB2):c.*609A>T rs4748485
NM_201596.3(CACNB2):c.*70_*71dup rs3841459
NM_201596.3(CACNB2):c.*995T>A rs189039831
NM_201596.3(CACNB2):c.1054+7C>T rs4314963
NM_201596.3(CACNB2):c.1206+6T>C rs147857449
NM_201596.3(CACNB2):c.1518C>T (p.Arg506=) rs34813638
NM_201596.3(CACNB2):c.1701C>T (p.Tyr567=) rs2228645
NM_201596.3(CACNB2):c.1785C>T (p.His595=) rs61733967
NM_201596.3(CACNB2):c.1794T>C (p.Ser598=) rs34503140
NM_201596.3(CACNB2):c.1965T>G (p.Asp655Glu) rs58225473

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