ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.2238A>T (p.Ser746=)

dbSNP: rs1553892658
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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 RCV000930186 SCV001075832 likely benign Gastrointestinal stromal tumor 2019-12-31 criteria provided, single submitter clinical testing

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