ClinVar Miner

Submissions for variant NM_006172.4(NPPA):c.426C>T (p.Ser142=)

dbSNP: rs747448548
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001174917 SCV001338352 likely benign not specified 2020-02-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002558780 SCV003268447 likely benign Atrial fibrillation, familial, 6 2022-01-23 criteria provided, single submitter clinical testing

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