ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A 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: 3
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NM_198056.2(SCN5A):c.2924G>A (p.Arg975Gln) rs753149586
NM_198056.2(SCN5A):c.3080G>A (p.Arg1027Gln) rs763891399
NM_198056.2(SCN5A):c.3118G>A (p.Gly1040Arg) rs199473186

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