ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.1627G>C (p.Val543Leu)

dbSNP: rs1958911016
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals RCV001175245 SCV001338822 uncertain significance Familial Mediterranean fever 2019-08-14 no assertion criteria provided clinical testing

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