ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.1866T>C (p.Asp622=)

gnomAD frequency: 0.05844  dbSNP: rs6000868
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001471493 SCV001675599 likely benign not provided 2023-11-27 criteria provided, single submitter clinical testing
GeneDx RCV001471493 SCV001857430 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001471493 SCV005206425 likely benign not provided criteria provided, single submitter not provided

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