ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.957T>C (p.Ser319=)

gnomAD frequency: 0.00008  dbSNP: rs375541232
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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 RCV002240275 SCV001661597 likely benign Gingival disorder 2024-01-21 criteria provided, single submitter clinical testing

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