ClinVar Miner

Submissions for variant NM_001113525.2(ZNF276):c.*1674G>C

gnomAD frequency: 0.00016  dbSNP: rs56216970
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000664586 SCV000788574 likely benign Fanconi anemia complementation group A 2017-01-27 criteria provided, single submitter clinical testing
ITMI RCV000122399 SCV000083950 not provided not specified 2013-09-19 no assertion provided reference population

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