ClinVar Miner

Submissions for variant NM_005373.3(MPL):c.1454C>T (p.Thr485Ile)

dbSNP: rs974626632
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001817721 SCV002069059 likely pathogenic not provided 2018-01-18 criteria provided, single submitter clinical testing

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