ClinVar Miner

Submissions for variant NM_001379500.1(COL18A1):c.2824_2837= (p.Gly942_Pro946=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001588004 SCV001821807 benign Knobloch syndrome 2021-07-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001588005 SCV001821808 benign Glaucoma, primary closed-angle 2021-07-22 criteria provided, single submitter clinical testing

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