ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1062C>G (p.Thr354=)

dbSNP: rs2109705643
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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 RCV002102252 SCV002329388 likely benign Gastrointestinal stromal tumor 2021-02-14 criteria provided, single submitter clinical testing

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