ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.2141+7C>T

gnomAD frequency: 0.00001  dbSNP: rs1360717801
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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 RCV000539911 SCV000630457 likely benign Gastrointestinal stromal tumor 2023-03-21 criteria provided, single submitter clinical testing

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