ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2015-16G>C

dbSNP: rs2039337410
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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 RCV002143025 SCV002450586 likely benign Fanconi anemia 2024-03-11 criteria provided, single submitter clinical testing

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