ClinVar Miner

List of variants in gene SCN3B reported as uncertain significance for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_018400.3(SCN3B):c.*1007dup rs72553907
NM_018400.3(SCN3B):c.*103C>T rs886047901
NM_018400.3(SCN3B):c.*104G>A rs886047900
NM_018400.3(SCN3B):c.*1095G>A rs558085329
NM_018400.3(SCN3B):c.*1151G>A rs72553906
NM_018400.3(SCN3B):c.*1318G>A rs77584352
NM_018400.3(SCN3B):c.*131T>A rs886047899
NM_018400.3(SCN3B):c.*1434G>A rs187400761
NM_018400.3(SCN3B):c.*1508A>G rs886047895
NM_018400.3(SCN3B):c.*1542A>C rs138774330
NM_018400.3(SCN3B):c.*1685A>G rs886047894
NM_018400.3(SCN3B):c.*1808G>A rs116885934
NM_018400.3(SCN3B):c.*1927A>G rs76257004
NM_018400.3(SCN3B):c.*1956_*1959delTATT rs776449566
NM_018400.3(SCN3B):c.*2056C>G rs886047893
NM_018400.3(SCN3B):c.*2178T>A rs148244106
NM_018400.3(SCN3B):c.*2203C>A rs543489443
NM_018400.3(SCN3B):c.*2266G>A rs75996884
NM_018400.3(SCN3B):c.*2366G>A rs867302682
NM_018400.3(SCN3B):c.*2429C>T rs886047892
NM_018400.3(SCN3B):c.*2603T>A rs886047891
NM_018400.3(SCN3B):c.*2629C>T rs886047890
NM_018400.3(SCN3B):c.*2798_*2800delGAA rs544984224
NM_018400.3(SCN3B):c.*3076C>T rs72552164
NM_018400.3(SCN3B):c.*3242G>A rs886047889
NM_018400.3(SCN3B):c.*3282T>C rs886047888
NM_018400.3(SCN3B):c.*3306G>A rs886047887
NM_018400.3(SCN3B):c.*3612A>G rs72552191
NM_018400.3(SCN3B):c.*4191C>A rs886047886
NM_018400.3(SCN3B):c.*4265C>A rs748097809
NM_018400.3(SCN3B):c.*4334C>T rs886047885
NM_018400.3(SCN3B):c.*4361T>C rs117409744
NM_018400.3(SCN3B):c.*4390C>T rs139934383
NM_018400.3(SCN3B):c.*4395G>A rs72552139
NM_018400.3(SCN3B):c.*4450G>A rs886047884
NM_018400.3(SCN3B):c.*447C>A rs80017720
NM_018400.3(SCN3B):c.*4523A>G rs114709124
NM_018400.3(SCN3B):c.*4537C>T rs758175811
NM_018400.3(SCN3B):c.*4541A>G rs144520035
NM_018400.3(SCN3B):c.*4588T>C rs765294617
NM_018400.3(SCN3B):c.*548C>T rs751005040
NM_018400.3(SCN3B):c.*657A>G rs886047898
NM_018400.3(SCN3B):c.*696A>G rs184556043
NM_018400.3(SCN3B):c.*869A>G rs72553909
NM_018400.3(SCN3B):c.*888A>G rs886047897
NM_018400.3(SCN3B):c.*930A>G rs555303241
NM_018400.3(SCN3B):c.-249G>T rs370826688
NM_018400.3(SCN3B):c.-252G>T rs577244366
NM_018400.3(SCN3B):c.-253G>C rs72552158
NM_018400.3(SCN3B):c.-332G>A rs886047903
NM_018400.3(SCN3B):c.-339C>G rs111341342
NM_018400.3(SCN3B):c.-393C>A rs547303769
NM_018400.3(SCN3B):c.-431G>A rs72552193
NM_018400.3(SCN3B):c.-43G>A rs72552185
NM_018400.3(SCN3B):c.-461del rs886047904
NM_018400.3(SCN3B):c.-489G>T rs886047905
NM_018400.3(SCN3B):c.-538G>A rs72552194
NM_018400.3(SCN3B):c.-557C>T rs72552195
NM_018400.3(SCN3B):c.-725C>G rs886047906
NM_018400.3(SCN3B):c.-736G>C rs886047907
NM_018400.3(SCN3B):c.-85G>T rs886047902
NM_018400.3(SCN3B):c.-9C>T rs553042856
NM_018400.3(SCN3B):c.29T>C (p.Leu10Pro) rs121918282
NM_018400.3(SCN3B):c.394C>T (p.Arg132Trp)
NM_018400.3(SCN3B):c.395G>A (p.Arg132Gln)
NM_018400.3(SCN3B):c.583G>A (p.Ala195Thr)
NM_018400.3(SCN3B):c.632T>G (p.Val211Gly)
NM_018400.3(SCN3B):c.93G>A (p.Ser31=) rs753258598
NM_018400.3(SCN3B):c.98C>T (p.Thr33Met)

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