ClinVar Miner

List of variants reported as likely benign for Brugada syndrome 4 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
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.804+653G>A rs142899184 0.00292
NM_201596.3(CACNB2):c.1560T>C (p.Pro520=) rs150280879 0.00099
NM_201596.3(CACNB2):c.590C>T (p.Ser197Phe) rs150528041 0.00064
NM_201596.3(CACNB2):c.1670C>T (p.Ser557Leu) rs137886839

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