ClinVar Miner

Submissions for variant NM_020066.5(FMN2):c.883T>C (p.Ser295Pro)

gnomAD frequency: 0.00575  dbSNP: rs201538863
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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) RCV000379986 SCV000340467 uncertain significance not provided 2016-03-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000379986 SCV001024177 benign not provided 2023-10-11 criteria provided, single submitter clinical testing

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