ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1360-4A>G

dbSNP: rs746911316
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000537057 SCV000626145 likely benign Fanconi anemia 2024-01-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506289 SCV002810068 likely benign Fanconi anemia complementation group A 2022-04-19 criteria provided, single submitter clinical testing

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