ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.6472+15_6472+16insC

dbSNP: rs149021782
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249508 SCV000306113 benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000249508 SCV000341888 benign not specified 2016-06-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057427 SCV002395474 benign not provided 2024-01-15 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002057427 SCV003916372 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing TRIOBP: BS2

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