ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.1386C>T (p.Thr462=)

gnomAD frequency: 0.00003  dbSNP: rs369645951
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001486356 SCV001690812 likely benign Atrial fibrillation, familial, 7 2020-04-14 criteria provided, single submitter clinical testing

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