ClinVar Miner

Submissions for variant NM_000243.2(MEFV):c.1179C>T (p.Pro393=) (rs104895082)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000083685 SCV001038563 likely benign Familial Mediterranean fever 2019-12-31 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001192541 SCV001360753 likely benign not specified 2020-01-31 criteria provided, single submitter clinical testing
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000083685 SCV000115772 not provided Familial Mediterranean fever no assertion provided not provided

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