ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.555C>T (p.Asn185=)

gnomAD frequency: 0.00004  dbSNP: rs539893573
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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 RCV002091140 SCV002390144 likely benign Gingival disorder 2023-08-04 criteria provided, single submitter clinical testing

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