ClinVar Miner

Submissions for variant NM_000128.3(F11):c.1517A>G (p.Asp506Gly) (rs281875258)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666655 SCV000790984 uncertain significance Hereditary factor XI deficiency disease 2017-04-18 criteria provided, single submitter clinical testing
UniProtKB/Swiss-Prot RCV000059011 SCV000090532 not provided not provided no assertion provided not provided

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