ClinVar Miner

List of variants in gene SCN2B reported as uncertain significance for atrial fibrillation (disease)

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_004588.5(SCN2B):c.140G>A (p.Arg47His) rs17121818
NM_004588.5(SCN2B):c.250C>T (p.Arg84Cys) rs760669515
NM_004588.5(SCN2B):c.251G>A (p.Arg84His) rs201460753
NM_004588.5(SCN2B):c.25C>T (p.Arg9Cys) rs878854711
NM_004588.5(SCN2B):c.292C>G (p.Arg98Gly) rs771234231
NM_004588.5(SCN2B):c.349G>A (p.Val117Met) rs754755062
NM_004588.5(SCN2B):c.410G>A (p.Arg137His) rs878854712
NM_004588.5(SCN2B):c.449-2A>C rs1085307094
NM_004588.5(SCN2B):c.461G>A (p.Arg154Gln) rs753389706
NM_004588.5(SCN2B):c.578C>G (p.Thr193Arg) rs115353159
NM_004588.5(SCN2B):c.611C>T (p.Thr204Met)
NM_004588.5(SCN2B):c.632A>G (p.Asp211Gly) rs587777023
NM_004588.5(SCN2B):c.93G>T (p.Glu31Asp)

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