ClinVar Miner

Submissions for variant NM_005431.2(XRCC2):c.39+8C>G

gnomAD frequency: 0.00006  dbSNP: rs200363289
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000226875 SCV000288891 likely benign not provided 2023-12-20 criteria provided, single submitter clinical testing
Mendelics RCV000988021 SCV001137568 likely benign Fanconi anemia complementation group U 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV000226875 SCV001887620 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000988021 SCV004016295 likely benign Fanconi anemia complementation group U 2023-07-07 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000226875 SCV004221583 benign not provided 2022-08-17 criteria provided, single submitter clinical testing

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