ClinVar Miner

Submissions for variant NM_015335.5(MED13L):c.2013-10del

dbSNP: rs542425590
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 RCV001649330 SCV001863003 benign not provided 2019-08-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005094857 SCV005769521 benign Transposition of the great arteries, dextro-looped 2024-09-24 criteria provided, single submitter clinical testing

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