ClinVar Miner

Submissions for variant NM_001277313.2(FMN1):c.3974A>G (p.Gln1325Arg)

gnomAD frequency: 0.00078  dbSNP: rs147769257
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000174703 SCV000226057 uncertain significance not provided 2016-08-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000174703 SCV001081018 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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