ClinVar Miner

Submissions for variant NM_006172.4(NPPA):c.93C>A (p.Ala31=)

dbSNP: rs374257969
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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 RCV001455446 SCV001659206 likely benign Atrial fibrillation, familial, 6 2023-10-06 criteria provided, single submitter clinical testing

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