ClinVar Miner

Submissions for variant NM_006894.5(FMO3):c.769G>A (p.Val257Met) (rs1736557)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000017698 SCV000351247 likely benign Trimethylaminuria 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000017698 SCV000037975 pathogenic Trimethylaminuria 2017-03-26 no assertion criteria provided literature only
PreventionGenetics RCV000253910 SCV000311644 benign not specified criteria provided, single submitter clinical testing

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