ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.639C>T (p.Pro213=)

gnomAD frequency: 0.00009  dbSNP: rs141229910
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002241020 SCV001703644 likely benign Gingival disorder 2024-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704627 SCV005205936 likely benign not provided criteria provided, single submitter not provided

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