ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1863T>C (p.Ala621=)

dbSNP: rs759613218
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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 RCV000465645 SCV000560726 likely benign Gastrointestinal stromal tumor 2020-07-02 criteria provided, single submitter clinical testing

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