ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A reported as benign for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_000335.4(SCN5A):c.2788-6C>T rs41260344
NM_000335.4(SCN5A):c.3048G>A (p.Thr1016=) rs376734571
NM_000335.4(SCN5A):c.3243G>A (p.Val1081=) rs41312407
NM_000335.4(SCN5A):c.3246C>T (p.Ser1082=) rs111422496
NM_000335.4(SCN5A):c.3266C>T (p.Pro1089Leu) rs1805125
NM_000335.4(SCN5A):c.3305C>A (p.Ser1102Tyr) rs7626962
NM_000335.4(SCN5A):c.3360G>A (p.Ala1120=) rs9858585

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