ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.1494T>C (p.Tyr498=)

dbSNP: rs2141669050
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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 RCV002088243 SCV002377182 likely benign Familial Mediterranean fever 2021-08-13 criteria provided, single submitter clinical testing

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