ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.3309C>T (p.His1103=)

gnomAD frequency: 0.00082  dbSNP: rs199594270
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000360902 SCV000343744 uncertain significance not provided 2016-08-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000360902 SCV001153688 likely benign not provided 2017-12-01 criteria provided, single submitter clinical testing
GeneDx RCV000360902 SCV001767679 likely benign not provided 2020-12-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000360902 SCV002460599 likely benign not provided 2023-10-24 criteria provided, single submitter clinical testing

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