ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.1135-25G>A

gnomAD frequency: 0.06159  dbSNP: rs201770712
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987096 SCV001136294 benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711497 SCV005262575 likely benign not provided criteria provided, single submitter not provided

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