ClinVar Miner

Submissions for variant NM_015335.5(MED13L):c.2013-29dup

dbSNP: rs542425590
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
GeneDx RCV001649087 SCV001863568 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001821938 SCV002069410 benign not specified 2019-05-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506707 SCV002805932 likely benign Cardiac anomalies - developmental delay - facial dysmorphism syndrome 2021-09-13 criteria provided, single submitter clinical testing

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