ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.5341-19G>A

gnomAD frequency: 0.00014  dbSNP: rs375732305
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001988935 SCV002287246 likely benign Fanconi anemia 2023-02-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002497980 SCV002796438 likely benign Spermatogenic failure 28; Premature ovarian failure 15 2022-01-13 criteria provided, single submitter clinical testing

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