ClinVar Miner

Submissions for variant NM_006172.4(NPPA):c.252C>T (p.Thr84=)

gnomAD frequency: 0.00004  dbSNP: rs755212754
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000230212 SCV000289141 likely benign Atrial fibrillation, familial, 6 2022-10-03 criteria provided, single submitter clinical testing

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