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%

Rare variants in genes of kidney and urinary tract development and copy number variants make up the current genetic arch

A source reports “20%” in the context of kidney: “Rare variants in genes of kidney and urinary tract development and copy number variants make up the current genetic architecture of CAKUT Given the early observations of familial segregation in 15-20% of CAKUT cases [ 1 , 2 , 8 ], a genetic basis for abnormal ”

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Generated 2026-11-13, last changed yesterday. Dedup key freq:20%. 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 (3 quotes)

Clinical characteristics and etiologies of hypomagnesemia in children: a single-center retrospective cohort study peer_reviewed · published 2026-01-01 · live page
Hypomagnesemia is common in critically ill adults, affecting 10-20% of hospitalized patients and over 50% of ICU patients [ 9 , 10 ].
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions peer_reviewed · published 2024-01-01 · live page
Graphical abstract Graphical abstract Keywords HNF1B -related disease is identified in 20% to 30% of fetuses with renal abnormalities.
Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract peer_reviewed · published 2024-01-01 · live page
Rare variants in genes of kidney and urinary tract development and copy number variants make up the current genetic architecture of CAKUT Given the early observations of familial segregation in 15-20% of CAKUT cases [ 1 , 2 , 8 ], a genetic basis for abnormal kidney and urinary tract development has long been proposed.

Supporting documents (3)

StorySourcePublishedSeenRelevance
Clinical characteristics and etiologies of hypomagnesemia in childr... pmc 2026-01-01 yesterday 1.00
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and... pmc 2024-01-01 yesterday 1.00
Translational strategies to uncover the etiology of congenital anom... pmc 2024-01-01 yesterday 1.00