ClinVar Miner

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

dbSNP: rs373954227
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001506191 SCV001711109 likely benign Fanconi anemia 2024-01-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501734 SCV002809540 likely benign Fanconi anemia complementation group A 2022-02-09 criteria provided, single submitter clinical testing

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