ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3409-18C>T

dbSNP: rs762166434
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002105552 SCV002397954 likely benign Fanconi anemia 2023-10-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494237 SCV002802649 likely benign Fanconi anemia complementation group A 2021-08-20 criteria provided, single submitter clinical testing

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