ClinVar Miner

Submissions for variant NM_000383.4(AIRE):c.783C>T (p.Ala261=)

dbSNP: rs777866382
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000975876 SCV001123768 likely benign Polyglandular autoimmune syndrome, type 1 2023-09-21 criteria provided, single submitter clinical testing
Natera, Inc. RCV000975876 SCV002083873 likely benign Polyglandular autoimmune syndrome, type 1 2020-10-30 no assertion criteria provided clinical testing

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