ClinVar Miner

Submissions for variant NM_001002294.3(FMO3):c.585G>C (p.Ser195=)

dbSNP: rs144283823
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244370 SCV000311642 likely benign not specified criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494744 SCV002794764 likely benign Trimethylaminuria 2022-01-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003546496 SCV004269330 benign not provided 2024-01-30 criteria provided, single submitter clinical testing

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