ClinVar Miner

Submissions for variant NM_001288705.3(CSF1R):c.1626+13G>A

gnomAD frequency: 0.00429  dbSNP: rs115895865
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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 RCV001795677 SCV002405416 benign not provided 2024-01-18 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001795677 SCV002035227 likely benign not provided no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001795677 SCV002036702 likely benign not provided no assertion criteria provided clinical testing

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