ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3721-7C>T

gnomAD frequency: 0.00001  dbSNP: rs1434575390
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503913 SCV000594725 uncertain significance not specified 2016-05-18 criteria provided, single submitter clinical testing
Invitae RCV000865535 SCV001006522 likely benign not provided 2017-12-19 criteria provided, single submitter clinical testing

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