ClinVar Miner

Submissions for variant NM_020661.4(AICDA):c.156+11A>C

gnomAD frequency: 0.00001  dbSNP: rs991275648
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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 RCV002122597 SCV002404781 likely benign Hyper-IgM syndrome type 2 2023-07-25 criteria provided, single submitter clinical testing

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