ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.511-45A>G

gnomAD frequency: 0.75732  dbSNP: rs554098
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252107 SCV000310553 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001532803 SCV001748526 benign Fanconi anemia complementation group G 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001597011 SCV001831117 benign not provided 2019-01-10 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV001532803 SCV004017685 benign Fanconi anemia complementation group G 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001597011 SCV005272595 benign not provided criteria provided, single submitter not provided

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