ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.2436T>C (p.Gly812=)

dbSNP: rs2109801609
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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 RCV001479853 SCV001684159 likely benign Gastrointestinal stromal tumor 2020-07-13 criteria provided, single submitter clinical testing

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