ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.1260+92G>A

gnomAD frequency: 0.00590  dbSNP: rs104895209
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001664394 SCV001872375 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001664394 SCV005293869 benign not provided criteria provided, single submitter not provided
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000083688 SCV000115776 not provided Familial Mediterranean fever no assertion provided not provided

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