ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.3332-33C>T

gnomAD frequency: 0.10043  dbSNP: rs10866507
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001676631 SCV001893219 benign not provided 2018-07-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838761 SCV002098742 benign Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome 2021-09-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838762 SCV002098743 benign Intellectual developmental disorder, autosomal dominant 63, with macrocephaly 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001676631 SCV005306147 benign not provided criteria provided, single submitter not provided

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