ClinVar Miner

Submissions for variant NM_015294.6(TRIM37):c.810-13dup

dbSNP: rs367700401
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000296131 SCV000404363 uncertain significance Mulibrey nanism syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000676024 SCV001764903 likely benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Invitae RCV000676024 SCV002408809 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676024 SCV000801758 likely benign not provided 2018-03-01 no assertion criteria provided clinical testing

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