ClinVar Miner

List of variants studied for Brugada syndrome 7

Included ClinVar conditions (2):
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Total variants: 24
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HGVS dbSNP
NC_000011.10:g.123642481G>A
NC_000011.10:g.123645646C>T
NM_018400.3(SCN3B):c.105C>T (p.Ala35=) rs368979661
NM_018400.3(SCN3B):c.161T>G (p.Val54Gly) rs587777555
NM_018400.3(SCN3B):c.17G>A (p.Arg6Lys) rs587777558
NM_018400.3(SCN3B):c.198C>T (p.Pro66=) rs115752338
NM_018400.3(SCN3B):c.249G>A (p.Glu83=) rs199974089
NM_018400.3(SCN3B):c.29T>C (p.Leu10Pro) rs121918282
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.389C>T (p.Ala130Val) rs587777556
NM_018400.3(SCN3B):c.390G>A (p.Ala130=) rs148484744
NM_018400.3(SCN3B):c.394C>T (p.Arg132Trp) rs371558196
NM_018400.3(SCN3B):c.395G>A (p.Arg132Gln) rs755967151
NM_018400.3(SCN3B):c.396G>T (p.Arg132=) rs752593287
NM_018400.3(SCN3B):c.416G>A (p.Arg139Gln) rs770801747
NM_018400.3(SCN3B):c.438C>T (p.Thr146=) rs1275085
NM_018400.3(SCN3B):c.445+8T>C rs759996960
NM_018400.3(SCN3B):c.482T>C (p.Met161Thr) rs587777557
NM_018400.3(SCN3B):c.582C>T (p.Asn194=) rs34964168
NM_018400.3(SCN3B):c.583G>A (p.Ala195Thr) rs375755770
NM_018400.3(SCN3B):c.585-4A>G rs745830643
NM_018400.3(SCN3B):c.632T>G (p.Val211Gly) rs750969469
NM_018400.3(SCN3B):c.98C>T (p.Thr33Met) rs140041927

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