ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.2352T>A (p.Ile784=)

dbSNP: rs2507442642
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002776197 SCV003030963 likely benign Fanconi anemia 2022-06-21 criteria provided, single submitter clinical testing

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