ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.2811C>T (p.Ile937=)

gnomAD frequency: 0.00111  dbSNP: rs115800799
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000350127 SCV000343280 uncertain significance not provided 2016-07-19 criteria provided, single submitter clinical testing
GeneDx RCV000350127 SCV001826989 likely benign not provided 2021-01-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000350127 SCV002394707 benign not provided 2022-01-13 criteria provided, single submitter clinical testing

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