ClinVar Miner

Submissions for variant NM_015599.3(PGM3):c.1539+19A>G

gnomAD frequency: 0.00694  dbSNP: rs115918938
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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 RCV001515338 SCV001723390 benign Immunodeficiency 23 2024-01-31 criteria provided, single submitter clinical testing

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