ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.114+16A>G

gnomAD frequency: 0.00015  dbSNP: rs117561671
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001596500 SCV001830871 likely benign not provided 2020-06-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001596500 SCV002929655 benign not provided 2023-10-05 criteria provided, single submitter clinical testing

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