ClinVar Miner

Submissions for variant NM_015599.3(PGM3):c.907_919del (p.Thr303fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005045860 SCV005674023 likely pathogenic Immunodeficiency 23 2024-03-15 criteria provided, single submitter clinical testing

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