ClinVar Miner

Submissions for variant NM_015294.6(TRIM37):c.810-3del

dbSNP: rs367700401
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000348619 SCV000404364 uncertain significance Mulibrey nanism syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000676023 SCV002410739 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676023 SCV000801757 benign not provided 2015-10-21 no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000676023 SCV001798583 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579489 SCV001807451 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001579489 SCV001928942 benign not specified no assertion criteria provided clinical testing

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