ClinVar Miner

Submissions for variant NM_006172.4(NPPA):c.94G>A (p.Val32Met)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001521904 SCV001731324 benign Atrial fibrillation, familial, 6 2020-12-08 criteria provided, single submitter clinical testing
GeneDx RCV001536622 SCV001753403 benign not provided 2019-07-30 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 16368448, 25854761, 17984371, 20543198, 20064500)

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