ClinVar Miner

Submissions for variant NM_000243.3(MEFV):c.318G>A (p.Ala106=)

gnomAD frequency: 0.00002  dbSNP: rs777765016
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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 RCV002210820 SCV002492561 likely benign Familial Mediterranean fever 2024-01-31 criteria provided, single submitter clinical testing

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