ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1115+12A>G

gnomAD frequency: 0.00007  dbSNP: rs745596772
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002117279 SCV002409252 likely benign Gastrointestinal stromal tumor 2024-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711816 SCV005257366 likely benign not provided criteria provided, single submitter not provided

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