ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.145+15T>C

dbSNP: rs780116924
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989959 SCV001140710 likely benign Fanconi anemia complementation group O 2019-05-28 criteria provided, single submitter clinical testing
Invitae RCV000989959 SCV003474825 likely benign Fanconi anemia complementation group O 2022-08-06 criteria provided, single submitter clinical testing

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