ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.5153+19T>C

gnomAD frequency: 0.00002  dbSNP: rs374696176
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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 RCV002143897 SCV002467546 likely benign Fanconi anemia 2023-12-12 criteria provided, single submitter clinical testing

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