ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1648-10C>T

gnomAD frequency: 0.00001  dbSNP: rs1198418224
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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 RCV001422485 SCV001625036 likely benign Gastrointestinal stromal tumor 2022-10-10 criteria provided, single submitter clinical testing

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