ClinVar Miner

List of variants in gene SCN1B reported as uncertain significance for atrial fibrillation (disease)

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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NM_001037.5(SCN1B):c.134G>A (p.Arg45His) rs180943300
NM_001037.5(SCN1B):c.158C>A (p.Thr53Asn) rs1568348711
NM_001037.5(SCN1B):c.347C>T (p.Ser116Leu)
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro) rs786205834
NM_001037.5(SCN1B):c.448+193G>A rs66876876

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