ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.84+53G>T

dbSNP: rs1563987651
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000714833 SCV000845570 uncertain significance Fanconi anemia complementation group G 2018-08-07 criteria provided, single submitter clinical testing

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