ClinVar Miner

Submissions for variant NM_006172.4(NPPA):c.264C>T (p.Ser88=)

dbSNP: rs1645075676
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001425362 SCV001627989 likely benign Atrial fibrillation, familial, 6 2019-06-13 criteria provided, single submitter clinical testing

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