ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.955A>C (p.Ser319Arg)

dbSNP: rs1599806193
Minimum review status: Collection method:
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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 RCV002240319 SCV001215218 uncertain significance Gingival disorder 2021-09-02 criteria provided, single submitter clinical testing

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