ClinVar Miner

List of variants in gene SCN2B reported as likely benign for atrial fibrillation

Included ClinVar conditions (51):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_004588.5(SCN2B):c.126T>C (p.Asn42=) rs376336851 0.00015
NM_004588.5(SCN2B):c.611C>T (p.Thr204Met) rs140034265 0.00013
NM_004588.5(SCN2B):c.129C>T (p.Gly43=) rs150955748 0.00009
NM_004588.5(SCN2B):c.357G>A (p.Pro119=) rs149169244 0.00008
NM_004588.5(SCN2B):c.135C>T (p.Asp45=) rs533110688 0.00007
NM_004588.5(SCN2B):c.470C>T (p.Thr157Met) rs760333798 0.00006
NM_004588.5(SCN2B):c.477C>T (p.Ala159=) rs777479532 0.00006
NM_004588.5(SCN2B):c.356C>T (p.Pro119Leu) rs767589740 0.00004
NM_004588.5(SCN2B):c.496G>A (p.Val166Ile) rs140314864 0.00003
NM_004588.5(SCN2B):c.523T>C (p.Leu175=) rs757644485 0.00002
NM_004588.5(SCN2B):c.615C>T (p.Asp205=) rs201971719 0.00002
NM_004588.5(SCN2B):c.70+15T>C rs899592055 0.00002
NM_004588.5(SCN2B):c.150C>T (p.Cys50=) rs751437266 0.00001
NM_004588.5(SCN2B):c.156C>T (p.Phe52=) rs961279155 0.00001
NM_004588.5(SCN2B):c.237+19G>A rs371565413 0.00001
NM_004588.5(SCN2B):c.324C>T (p.Tyr108=) rs981151593 0.00001
NM_004588.5(SCN2B):c.327T>C (p.Asp109=) rs776528668 0.00001
NM_004588.5(SCN2B):c.340C>T (p.Leu114=) rs961380475 0.00001
NM_004588.5(SCN2B):c.348C>T (p.Asn116=) rs72544144 0.00001
NM_004588.5(SCN2B):c.354G>A (p.Gln118=) rs752863331 0.00001
NM_004588.5(SCN2B):c.39C>T (p.Ser13=) rs772656576 0.00001
NM_004588.5(SCN2B):c.408C>T (p.His136=) rs780138122 0.00001
NM_004588.5(SCN2B):c.639C>T (p.Gly213=) rs371409245 0.00001
NM_004588.5(SCN2B):c.108C>T (p.Ala36=)
NM_004588.5(SCN2B):c.111C>T (p.Thr37=)
NM_004588.5(SCN2B):c.114C>T (p.Leu38=) rs1478317204
NM_004588.5(SCN2B):c.117C>T (p.Asn39=)
NM_004588.5(SCN2B):c.144G>A (p.Leu48=) rs2135518426
NM_004588.5(SCN2B):c.159C>T (p.Asn53=)
NM_004588.5(SCN2B):c.238-18C>T
NM_004588.5(SCN2B):c.238-6C>T rs200842493
NM_004588.5(SCN2B):c.268C>T (p.Leu90=)
NM_004588.5(SCN2B):c.303C>T (p.Phe101=)
NM_004588.5(SCN2B):c.321G>A (p.Lys107=)
NM_004588.5(SCN2B):c.396C>T (p.Pro132=)
NM_004588.5(SCN2B):c.448+13G>A
NM_004588.5(SCN2B):c.449-13_449-12delinsAA rs2135517612
NM_004588.5(SCN2B):c.449-15C>T
NM_004588.5(SCN2B):c.45G>A (p.Thr15=) rs376823705
NM_004588.5(SCN2B):c.495C>T (p.Ser165=) rs1217452578
NM_004588.5(SCN2B):c.498C>G (p.Val166=) rs200709238
NM_004588.5(SCN2B):c.508C>T (p.Leu170=)
NM_004588.5(SCN2B):c.51C>A (p.Leu17=)
NM_004588.5(SCN2B):c.529C>T (p.Leu177=)
NM_004588.5(SCN2B):c.546T>C (p.Cys182=)
NM_004588.5(SCN2B):c.561A>G (p.Lys187=) rs1336662030
NM_004588.5(SCN2B):c.567G>A (p.Gln189=) rs2135517512
NM_004588.5(SCN2B):c.585C>T (p.Asp195=)
NM_004588.5(SCN2B):c.594C>T (p.Thr198=) rs1326811641
NM_004588.5(SCN2B):c.630G>A (p.Pro210=) rs751230713
NM_004588.5(SCN2B):c.67T>C (p.Leu23=) rs2134623717
NM_004588.5(SCN2B):c.70+14A>T
NM_004588.5(SCN2B):c.70+17T>C
NM_004588.5(SCN2B):c.81A>G (p.Gly27=)
NM_004588.5(SCN2B):c.96C>A (p.Val32=)

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