ClinVar Miner

Submissions for variant NM_005431.2(XRCC2):c.794T>C (p.Leu265Ser)

dbSNP: rs771671971
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000709046 SCV000838280 uncertain significance Hereditary cancer-predisposing syndrome 2018-07-02 criteria provided, single submitter clinical testing
Mendelics RCV000988010 SCV001137556 uncertain significance Fanconi anemia complementation group U 2019-05-28 criteria provided, single submitter clinical testing

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