ClinVar Miner

Submissions for variant NM_001129.5(AEBP1):c.863-37dup

dbSNP: rs58863562
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
Genome-Nilou Lab RCV001549258 SCV001769378 benign Ehlers-Danlos syndrome, classic-like, 2 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001647423 SCV001860849 benign not provided 2019-10-02 criteria provided, single submitter clinical testing

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