ClinVar Miner

Submissions for variant NM_006172.4(NPPA):c.351G>A (p.Ala117=)

dbSNP: rs1473148185
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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 RCV002182714 SCV002344394 likely benign Atrial fibrillation, familial, 6 2021-06-04 criteria provided, single submitter clinical testing

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