ClinVar Miner

Submissions for variant NM_001002841.1(MYL4):c.31G>A (p.Glu11Lys) (rs886037778)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000415520 SCV000493917 pathogenic Atrial fibrillation, familial, 18 2016-12-28 no assertion criteria provided literature only
Toronto General Hospital,University of Toronto RCV000240709 SCV000264340 pathogenic Familial atrial fibrillation 2016-02-26 no assertion criteria provided research

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