ClinVar Miner

Submissions for variant NM_000460.4(THPO):c.229-17_229-14dup

dbSNP: rs55827759
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244455 SCV000304403 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000343127 SCV000442366 likely benign Thrombocythemia 1 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001567825 SCV001791580 likely benign not provided 2019-01-20 criteria provided, single submitter clinical testing
Invitae RCV001567825 SCV002454273 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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