ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.2484+9C>A

dbSNP: rs2109802167
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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 RCV001492820 SCV001697440 likely benign Gastrointestinal stromal tumor 2022-08-10 criteria provided, single submitter clinical testing

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