ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.337+1_337+8dup

dbSNP: rs2109663204
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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 RCV001454065 SCV001657776 likely benign Gastrointestinal stromal tumor 2020-06-23 criteria provided, single submitter clinical testing

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