17q12, explained for kidsdeletion syndrome · static snapshot
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A number from a study Kidneys and diabetes 1 supporting source confidence 97% novelty 60%

Overall, 36/486 probands (7.4%) with genetically confirmed monogenic diabetes in the NMR carried a P/LP HNF1B sequence v

A source reports “7.4%” in the context of diabetes metabolic: “Overall, 36/486 probands (7.4%) with genetically confirmed monogenic diabetes in the NMR carried a P/LP HNF1B sequence variant or 17q12del.”

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How this was derived

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Generated 2026-11-13, last changed yesterday. Dedup key freq:7.4%. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childhood Diabetes Registry: Clinical Insights and Prevalence Informed by Genetic and Functional Evaluation peer_reviewed · published 2026-06-03 · live page
Overall, 36/486 probands (7.4%) with genetically confirmed monogenic diabetes in the NMR carried a P/LP HNF1B sequence variant or 17q12del.

Supporting documents (1)

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HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childho... openalex 2026-06-03 yesterday 1.00