ClinVar Miner

List of variants in gene SCN3B 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: 33
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HGVS dbSNP
NM_018400.3(SCN3B):c.*1232G>A rs72553903
NM_018400.3(SCN3B):c.*1257G>A rs72552202
NM_018400.3(SCN3B):c.*1289C>T rs72552201
NM_018400.3(SCN3B):c.*1290G>A rs72552200
NM_018400.3(SCN3B):c.*1686T>C rs41497645
NM_018400.3(SCN3B):c.*1746G>A rs10400374
NM_018400.3(SCN3B):c.*1856A>G rs76401585
NM_018400.3(SCN3B):c.*2174dup rs398088090
NM_018400.3(SCN3B):c.*2242C>T rs72552177
NM_018400.3(SCN3B):c.*2462G>A rs72552176
NM_018400.3(SCN3B):c.*2516G>A rs72552175
NM_018400.3(SCN3B):c.*2561C>T rs72552174
NM_018400.3(SCN3B):c.*2722G>A rs72552173
NM_018400.3(SCN3B):c.*3060G>T rs80274943
NM_018400.3(SCN3B):c.*3444A>T rs377271838
NM_018400.3(SCN3B):c.*3748G>A rs2027767
NM_018400.3(SCN3B):c.*3973_*3976del rs149550554
NM_018400.3(SCN3B):c.*4394C>T rs12286568
NM_018400.3(SCN3B):c.*509G>A rs72552198
NM_018400.3(SCN3B):c.*855A>C rs72553910
NM_018400.3(SCN3B):c.*892C>A rs115252019
NM_018400.3(SCN3B):c.-179C>T rs72552156
NM_018400.3(SCN3B):c.-181A>G rs3851103
NM_018400.3(SCN3B):c.-194G>T rs72552157
NM_018400.3(SCN3B):c.-234G>A rs3851104
NM_018400.3(SCN3B):c.-364G>A rs67792557
NM_018400.3(SCN3B):c.-692G>C rs7483687
NM_018400.3(SCN3B):c.-763G>A rs12420563
NM_018400.3(SCN3B):c.105C>T (p.Ala35=) rs368979661
NM_018400.3(SCN3B):c.198C>T (p.Pro66=) rs115752338
NM_018400.3(SCN3B):c.327C>T (p.Asn109=) rs199937307
NM_018400.3(SCN3B):c.328G>A (p.Val110Ile) rs147205617
NM_018400.3(SCN3B):c.438C>T (p.Thr146=) rs1275085

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