ClinVar Miner

Submissions for variant NM_018062.4(FANCL):c.776-8A>T

dbSNP: rs753745302
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000900805 SCV001045145 likely benign Fanconi anemia 2023-07-07 criteria provided, single submitter clinical testing

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