ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3408+45G>A

gnomAD frequency: 0.05862  dbSNP: rs1800355
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000254260 SCV000302493 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001610558 SCV001833663 benign not provided 2019-02-02 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316336 SCV004017544 benign Fanconi anemia complementation group A 2023-07-07 criteria provided, single submitter clinical testing

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