ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.876C>G (p.Ala292=)

dbSNP: rs2109693552
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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 RCV002156374 SCV002471158 likely benign Gastrointestinal stromal tumor 2022-05-24 criteria provided, single submitter clinical testing

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