ClinVar Miner

Submissions for variant NM_000383.4(AIRE):c.1207G>A (p.Ala403Thr)

dbSNP: rs543891914
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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 RCV000633452 SCV000754679 benign Polyglandular autoimmune syndrome, type 1 2024-01-04 criteria provided, single submitter clinical testing

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