ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1576C>T (p.Leu526=)

dbSNP: rs1553891660
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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 RCV000550703 SCV000630426 likely benign Gastrointestinal stromal tumor 2017-04-03 criteria provided, single submitter clinical testing

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