ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.1356A>G (p.Leu452=)

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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 RCV005081969 SCV005724333 likely benign not provided 2024-04-25 criteria provided, single submitter clinical testing

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