ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.347+3A>G

gnomAD frequency: 0.00665  dbSNP: rs16903358
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 RCV000972730 SCV001120454 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000972730 SCV001803578 likely benign not provided 2020-12-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000972730 SCV005259668 likely benign not provided criteria provided, single submitter not provided

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