17q12 Knowledge Basedeletion syndrome · static snapshot
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Frequency / statistic kidney and urinary tract 1 supporting source confidence 97% novelty 60%

A study of 29 stillbirth fetuses with renal agenesis identified a heterozygous RET mutation in 7/19 (37%) of those with

A source reports “37%” in the context of kidney: “A study of 29 stillbirth fetuses with renal agenesis identified a heterozygous RET mutation in 7/19 (37%) of those with BRA and in 2/10 (20%) of those with URA ( 31 ), ranking RET among the most frequent genes reported in BRA.”

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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 yesterday. Dedup key freq:37%. 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)

The genetic etiologies of bilateral renal agenesis peer_reviewed · published 2024-01-01 · live page
A study of 29 stillbirth fetuses with renal agenesis identified a heterozygous RET mutation in 7/19 (37%) of those with BRA and in 2/10 (20%) of those with URA ( 31 ), ranking RET among the most frequent genes reported in BRA.

Supporting documents (1)

ArticleSourcePublishedSeenRelevance
The genetic etiologies of bilateral renal agenesis pmc 2024-01-01 yesterday 1.00