ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1653C>T (p.Pro551=)

dbSNP: rs2109775577
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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 RCV001468127 SCV001672165 likely benign Gastrointestinal stromal tumor 2022-05-15 criteria provided, single submitter clinical testing

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