ClinVar Miner

Submissions for variant NM_032578.3(MYPN):c.1585C>T (p.Gln529Ter) (rs199476408)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Leiden Muscular Dystrophy (MYPN) RCV000024509 SCV000045813 not provided not provided 2012-04-27 no assertion provided curation
OMIM RCV000043547 SCV000071260 pathogenic Cardiomyopathy, familial restrictive, 4 2012-05-01 no assertion criteria provided literature only

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