ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1991-10G>C

dbSNP: rs1577997814
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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 RCV000983246 SCV001131267 likely benign Gastrointestinal stromal tumor 2023-06-11 criteria provided, single submitter clinical testing

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