ClinVar Miner

Submissions for variant NM_001288705.3(CSF1R):c.93C>T (p.Val31=)

dbSNP: rs41424646
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515107 SCV001723105 benign not provided 2024-11-10 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001515107 SCV002035155 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001515107 SCV002038315 likely benign not provided no assertion criteria provided clinical testing

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