ClinVar Miner

Submissions for variant NM_000791.4(DHFR):c.-437GGGGCGCTG[1]

dbSNP: rs60484572
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000890699 SCV001034464 benign not provided 2018-04-04 criteria provided, single submitter clinical testing
GeneDx RCV000890699 SCV001834597 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001729736 SCV002047074 benign not specified 2021-05-11 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258028 SCV002536015 benign Hereditary cancer-predisposing syndrome 2021-06-13 criteria provided, single submitter curation
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV001729736 SCV002570206 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001729736 SCV001978767 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001729736 SCV001979940 benign not specified no assertion criteria provided clinical testing

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