ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.1397-15TA[6]

dbSNP: rs112326758
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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 RCV000241683 SCV000313694 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001683100 SCV001898423 benign not provided 2019-03-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701972 SCV001933298 benign Premature ovarian failure 15 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701905 SCV001933300 benign Spermatogenic failure 28 2021-08-10 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV001683100 SCV002011500 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Invitae RCV002058305 SCV002430058 benign Fanconi anemia 2024-02-01 criteria provided, single submitter clinical testing

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