ClinVar Miner

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

Included ClinVar conditions (44):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_005472.5(KCNE3):c.198T>C (p.Phe66=) rs2270676 0.12227
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_015141.4(GPD1L):c.370A>G (p.Ile124Val) rs72552293 0.00291
NM_201596.3(CACNB2):c.120+379A>G
NM_201596.3(CACNB2):c.1521C>T (p.Ser507=) rs143060134
NM_201596.3(CACNB2):c.1816C>G (p.Arg606Gly) rs61733968

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