ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1518T>C (p.Phe506=)

dbSNP: rs2109769728
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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 RCV002088734 SCV002388230 likely benign Gastrointestinal stromal tumor 2021-11-06 criteria provided, single submitter clinical testing

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