ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.1785T>C (p.Gly595=)

gnomAD frequency: 0.04913  dbSNP: rs2277045
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 RCV001649388 SCV001863072 benign not provided 2018-08-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001649388 SCV005306133 benign not provided criteria provided, single submitter not provided

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