ClinVar Miner

Submissions for variant NM_000222.2(KIT):c.1648_1674del

dbSNP: rs121913234
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000014871 SCV000035126 pathogenic Gastrointestinal stromal tumor 2005-06-16 no assertion criteria provided literature only

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