ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.2901C>T (p.Ser967=)

dbSNP: rs1553893836
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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 RCV001411326 SCV001613385 likely benign Gastrointestinal stromal tumor 2018-07-02 criteria provided, single submitter clinical testing

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