ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.894A>G (p.Pro298=)

dbSNP: rs1959077728
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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 RCV002120641 SCV002433158 likely benign Familial Mediterranean fever 2022-11-07 criteria provided, single submitter clinical testing

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