ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2601+9A>T

dbSNP: rs771837383
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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 RCV000502806 SCV000594633 uncertain significance not specified 2015-11-18 criteria provided, single submitter clinical testing
Invitae RCV000868476 SCV001009809 likely benign Fanconi anemia 2023-12-25 criteria provided, single submitter clinical testing

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