ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.618C>T (p.Phe206=)

dbSNP: rs2122322070
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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 RCV002243131 SCV001618426 likely benign Gingival disorder 2020-03-06 criteria provided, single submitter clinical testing

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