ClinVar Miner

Submissions for variant NM_000243.2(MEFV):c.372C>T (p.Pro124=) (rs104895078)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000507322 SCV000604192 benign not specified 2017-02-23 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000083771 SCV000396782 uncertain significance Familial Mediterranean fever 2016-06-14 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000586541 SCV000696070 uncertain significance not provided 2017-03-20 criteria provided, single submitter clinical testing
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000083771 SCV000115867 not provided Familial Mediterranean fever no assertion provided not provided

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