ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1901-1G>A

dbSNP: rs1485075318
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000669366 SCV000794113 likely pathogenic Fanconi anemia complementation group A 2017-09-11 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003237984 SCV002010196 likely pathogenic not provided 2021-11-03 criteria provided, single submitter clinical testing

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