ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.954C>G (p.Ala318=)

gnomAD frequency: 0.00002  dbSNP: rs766700447
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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 RCV002240596 SCV001678780 likely benign Gingival disorder 2020-08-06 criteria provided, single submitter clinical testing

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