ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.528C>T (p.Cys176=)

gnomAD frequency: 0.00001  dbSNP: rs769223294
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002112250 SCV002387700 likely benign Gingival disorder 2023-12-30 criteria provided, single submitter clinical testing

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