ClinVar Miner

Submissions for variant NM_000459.5(TEK):c.3062+38dup

dbSNP: rs57300282
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 RCV001838928 SCV002098670 benign Glaucoma 3, primary congenital, E 2021-09-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838927 SCV002098681 benign Multiple cutaneous and mucosal venous malformations 2021-09-10 criteria provided, single submitter clinical testing

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