ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.369C>T (p.Ser123=)

dbSNP: rs2109671998
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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 RCV001395334 SCV001597042 likely benign Gastrointestinal stromal tumor 2021-06-14 criteria provided, single submitter clinical testing

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