ClinVar Miner

List of variants in gene SCN1B reported as likely benign for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_001037.5(SCN1B):c.-27G>C rs758958222
NM_001037.5(SCN1B):c.-95C>T rs569134158
NM_001037.5(SCN1B):c.-9C>A rs66671189
NM_001037.5(SCN1B):c.207+14G>A rs16969924
NM_001037.5(SCN1B):c.258C>T (p.Phe86=) rs751009774
NM_001037.5(SCN1B):c.273G>A (p.Val91=) rs16969926
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser) rs72552027
NM_001037.5(SCN1B):c.351C>T (p.Gly117=) rs3746255
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile) rs72558029
NM_001037.5(SCN1B):c.448+163A>G rs761312032
NM_001037.5(SCN1B):c.448+215C>G rs1015574605
NM_001037.5(SCN1B):c.448+230C>T rs769132369
NM_001037.5(SCN1B):c.448+257G>C rs1040023313
NM_001037.5(SCN1B):c.448+308C>A rs986180682
NM_001037.5(SCN1B):c.448+311G>A rs1019053238
NM_001037.5(SCN1B):c.448+320C>T rs570257058
NM_001037.5(SCN1B):c.448+321G>A rs72558028
NM_001037.5(SCN1B):c.448+8G>C rs200222933
NM_001037.5(SCN1B):c.448+92C>A rs750396627
NM_001037.5(SCN1B):c.448+92C>G rs750396627
NM_001037.5(SCN1B):c.471C>T (p.Ile157=) rs765269835
NM_001037.5(SCN1B):c.501T>C (p.Ile167=) rs16969930
NM_001037.5(SCN1B):c.546C>T (p.Tyr182=) rs775659068
NM_001037.5(SCN1B):c.588T>C (p.Asn196=) rs77244433
NM_001037.5(SCN1B):c.632G>A (p.Cys211Tyr) rs150721582
NM_001037.5(SCN1B):c.63C>T (p.Cys21=) rs200339565
NM_001037.5(SCN1B):c.78G>A (p.Ser26=) rs774401364

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