ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.4516-5_4516-2del

dbSNP: rs796584585
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253891 SCV000313702 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000253891 SCV000603597 benign not specified 2016-12-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001521135 SCV001730406 benign Fanconi anemia 2025-02-04 criteria provided, single submitter clinical testing
GeneDx RCV001610720 SCV001840816 benign not provided 2019-03-08 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 33552906)
Genome-Nilou Lab RCV001702399 SCV001933307 benign Premature ovarian failure 15 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701907 SCV001933309 benign Spermatogenic failure 28 2021-08-10 criteria provided, single submitter clinical testing

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