ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.942C>T (p.His314=)

gnomAD frequency: 0.00003  dbSNP: rs749154560
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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 RCV002240883 SCV001699997 likely benign Gingival disorder 2023-05-29 criteria provided, single submitter clinical testing

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