ClinVar Miner

Submissions for variant NM_005431.2(XRCC2):c.39+8C>G (rs200363289)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000226875 SCV000288891 likely benign not provided 2019-12-31 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

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