ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.4058+38A>G

gnomAD frequency: 0.04152  dbSNP: rs10513177
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 RCV001672008 SCV001888162 benign not provided 2018-10-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001672008 SCV005306164 benign not provided criteria provided, single submitter not provided

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