ClinVar Miner

Submissions for variant NM_006074.5(TRIM22):c.247G>A (p.Glu83Lys)

gnomAD frequency: 0.00186  dbSNP: rs200668710
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Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV001795671 SCV005191134 uncertain significance not provided criteria provided, single submitter not provided
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001795671 SCV002035125 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001795671 SCV002037927 uncertain significance not provided no assertion criteria provided clinical testing

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