ClinVar Miner

Submissions for variant NM_002204.4(ITGA3):c.1469+10T>C (rs4793639)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000600838 SCV000733692 benign Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital no assertion criteria provided clinical testing

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