Varaico: Literature-Extracted Genetic Variants

Gene:CST3
Variant:p.H69_S70insG
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CST3

NM_000099.4:p.H69_S70insG

Associated Papers

HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.

Thomas R et al.

Pediatric Nephrology (berlin, Germany), 2011

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."