ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.646+58C>T

gnomAD frequency: 0.17456  dbSNP: rs17885726
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001532802 SCV001748525 benign Fanconi anemia complementation group G 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001720303 SCV001949014 benign not provided 2019-03-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001720303 SCV005272594 benign not provided criteria provided, single submitter not provided

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