ClinVar Miner

Submissions for variant NM_020066.5(FMN2):c.1689C>A (p.Ser563=)

gnomAD frequency: 0.00039  dbSNP: rs141488751
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000504362 SCV000594837 likely benign not specified 2016-01-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000981827 SCV001129835 likely benign not provided 2018-12-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000981827 SCV005257491 likely benign not provided criteria provided, single submitter not provided

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