ClinVar Miner

Submissions for variant NM_000883.4(IMPDH1):c.504+8A>G

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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 RCV002751437 SCV003026305 likely benign not provided 2022-01-04 criteria provided, single submitter clinical testing

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