ClinVar Miner

Submissions for variant NM_032578.3(MYPN):c.970C>T (p.His324Tyr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Klaassen Lab,Charite University Medicine Berlin RCV000853171 SCV000995886 uncertain significance Primary familial hypertrophic cardiomyopathy 2019-07-03 criteria provided, single submitter research

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