17q12, explained for kidsdeletion syndrome · static snapshot
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A number from a study What it can look like 1 supporting source confidence 97% novelty 60%

It's noteworthy that this form of liver disease is a predominant feature in approximately 65% of patients with spontaneo

A source reports “65%” in the context of hepatic: “It's noteworthy that this form of liver disease is a predominant feature in approximately 65% of patients with spontaneous HNF-1β gene mutations.”

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How this was derived

Numbers are quoted verbatim from the source; check the source before quoting onward.

Generated 2026-11-13, last changed today. Dedup key freq:65%. 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 (2 quotes)

Atypical presentation of HNF1β gene mutation mimicking type 2 diabetes: Case report and literature review peer_reviewed · published 2025-01-01 · live page
Hepatic dysfunction occurs in 65% of patients with mutations in the HNF1β gene.
A Case of 17q12 Microdeletion Syndrome in a MODY5 Type Diabetes with HNF-1β Gene Mutation Accompanied peer_reviewed · published 2024-01-01 · live page
It's noteworthy that this form of liver disease is a predominant feature in approximately 65% of patients with spontaneous HNF-1β gene mutations.

Supporting documents (2)

StorySourcePublishedSeenRelevance
Atypical presentation of HNF1β gene mutation mimicking type 2 diabe... pmc 2025-01-01 yesterday 1.00
A Case of 17q12 Microdeletion Syndrome in a MODY5 Type Diabetes wit... pmc 2024-01-01 yesterday 1.00