ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.553A>G (p.Asn185Asp)

gnomAD frequency: 0.00016  dbSNP: rs145973159
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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 RCV002243074 SCV001617434 likely benign Gingival disorder 2023-12-09 criteria provided, single submitter clinical testing

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