ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.2507C>T (p.Thr836Ile) (rs34338511)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000864926 SCV001005812 benign not provided 2018-09-11 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000864926 SCV001143371 benign not provided 2019-06-04 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001002049 SCV001159874 likely benign none provided 2020-05-11 criteria provided, single submitter clinical testing

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