ClinVar Miner

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

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
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.390G>A (p.Ala130=) rs148484744
NM_018400.3(SCN3B):c.582C>T (p.Asn194=) rs34964168

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