ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.26C>T (p.Thr9Met)

gnomAD frequency: 0.00215  dbSNP: rs148095693
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002231220 SCV000626487 likely benign Gingival disorder 2024-01-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001703188 SCV005205937 likely benign not provided criteria provided, single submitter not provided
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001703188 SCV001930078 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001703188 SCV001965849 likely benign not provided no assertion criteria provided clinical testing

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