ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.472T>C (p.Leu158=)

gnomAD frequency: 0.00002  dbSNP: rs1471159412
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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 RCV002241028 SCV001705583 likely benign Gingival disorder 2020-02-22 criteria provided, single submitter clinical testing

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