ClinVar Miner

List of variants in gene SCN3B reported as likely benign for Brugada syndrome 7

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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NM_018400.3(SCN3B):c.105C>T (p.Ala35=) rs368979661
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.396G>T (p.Arg132=) rs752593287
NM_018400.3(SCN3B):c.445+8T>C rs759996960
NM_018400.3(SCN3B):c.585-4A>G rs745830643

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