ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1360-12C>T

gnomAD frequency: 0.00001  dbSNP: rs951725614
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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 RCV001941332 SCV002218040 likely benign Fanconi anemia 2024-03-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002497822 SCV002808072 likely benign Fanconi anemia complementation group A 2021-12-15 criteria provided, single submitter clinical testing

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