ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.278-12T>C

gnomAD frequency: 0.00001  dbSNP: rs1018265024
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002112485 SCV002382235 likely benign Familial Mediterranean fever 2023-10-13 criteria provided, single submitter clinical testing

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