ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.42G>A (p.Gly14=)

gnomAD frequency: 0.00001  dbSNP: rs866728748
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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 RCV002240290 SCV001668428 likely benign Gingival disorder 2022-02-02 criteria provided, single submitter clinical testing

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