ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.6472+19_6472+20insA

gnomAD frequency: 0.00002  dbSNP: rs397769084
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000359137 SCV000341254 uncertain significance not provided 2016-05-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000359137 SCV004626672 likely benign not provided 2024-01-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000359137 SCV005194461 uncertain significance not provided criteria provided, single submitter not provided

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