17q12 Knowledge Basedeletion syndrome · static snapshot
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New publication Genes & inheritance 1 supporting source confidence 97% novelty 75%

HNF1B gene: MedlinePlus Genetics

HNF1B gene HNF1 homeobox B Normal Function The HNF1B gene provides instructions for making a protein called hepatocyte nuclear factor-1 beta (HNF-1β).

How this was derived

Indexed from **web** on 2026-11-13 (relevance 1.00, tier reference).

Generated 2026-11-13, last changed today. Dedup key newdoc:567. 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)

More About This Health Condition Congenital anomalies of kidney and urinary tract Mutations within the HNF1B gene are found in people with abnormalities of the kidneys and other structures of the urinary tract but without other features of 17q12 deletion syndrome (described above) or RCAD syndrome (described above).

Supporting documents (1)

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HNF1B gene: MedlinePlus Genetics web - today 1.00