ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.338-10G>T

dbSNP: rs1577956522
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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 RCV000980670 SCV001128626 likely benign Gastrointestinal stromal tumor 2019-11-16 criteria provided, single submitter clinical testing

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