ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.911-78T>C

gnomAD frequency: 0.01123  dbSNP: rs11466021
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001588912 SCV001816239 likely benign not provided 2018-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001588912 SCV005215125 likely benign not provided criteria provided, single submitter not provided
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000083805 SCV000115905 not provided Familial Mediterranean fever no assertion provided not provided

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