ClinVar Miner

Submissions for variant NM_174916.3(UBR1):c.735A>T (p.Leu245=)

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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 RCV003679282 SCV004400248 likely benign not provided 2023-02-06 criteria provided, single submitter clinical testing

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