ClinVar Miner

Submissions for variant NM_020661.4(AICDA):c.93C>T (p.Tyr31=)

gnomAD frequency: 0.00001  dbSNP: rs777729620
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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 RCV001470282 SCV001674377 likely benign Hyper-IgM syndrome type 2 2023-08-07 criteria provided, single submitter clinical testing

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