ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.*12T>C

gnomAD frequency: 0.00001  dbSNP: rs104895183
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000083676 SCV000115762 not provided Familial Mediterranean fever no assertion provided not provided

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