ClinVar Miner

Submissions for variant NM_002476.2(MYL4):c.447G>A (p.Thr149=) (rs371944933)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000946148 SCV001092250 likely benign Atrial fibrillation, familial, 18 2019-04-19 criteria provided, single submitter clinical testing

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