ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.1889G>A (p.Arg630His)

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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 RCV003820988 SCV004625214 likely benign not provided 2024-03-28 criteria provided, single submitter clinical testing

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