ClinVar Miner

Submissions for variant NM_015559.3(SETBP1):c.1159G>C (p.Val387Leu)

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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 RCV003574034 SCV004329232 benign not provided 2024-04-16 criteria provided, single submitter clinical testing

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