ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.5764C>T (p.Arg1922Trp)

gnomAD frequency: 0.00032  dbSNP: rs183941928
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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 RCV000252969 SCV000306111 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000927547 SCV001073132 benign not provided 2023-12-11 criteria provided, single submitter clinical testing
GeneDx RCV000927547 SCV001914657 benign not provided 2018-11-02 criteria provided, single submitter clinical testing

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