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Nephrotic Syndrome, Type 4, as genome-wide studies have reported it: 14 positions from 1 study. Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
This is the record of what genome-wide association studies have found for Nephrotic Syndrome, Type 4 (the GWAS Catalog's "Nephrotic syndrome, type 4"): 14 positions reported by 1 study. The page is put together by code from the catalogue's records and the studies' own listings, and it is rebuilt whenever the records change, so it always reflects them as they stand.
A study. The 14 positions on this page from it: rs121907900 (WT1), rs1554939785 (WT1), rs1554946480 (WT1), rs1590410578 (WT1), rs1853443391 (LOC107982234), rs2132897818 (WT1), rs2132898667 (WT1), rs2132914663 (WT1), and 6 more.
The catalogue maps the 14 positions to 2 genes: WT1, LOC107982234. That mapping says where a position sits, in a gene or beside one — not what it does. For what each study measured, follow its citation above.
Read this page as a list of findings about Nephrotic Syndrome, Type 4, not as an account of it. Each finding is a position that a genome-wide study linked to the condition across a population; the page adds no description, no prevalence and no advice, because the records hold none. The variant pages linked above give each study's record for its position, and ClinVar's where one exists.
Nephrotic Syndrome, Type 4 is diagnosed by a clinician — not from a genotype. None of the 14 variants on this page is used by any guideline to predict, screen for or diagnose it.
This page was assembled by code from association records. It holds no clinical guidance, because its sources hold none: a genome-wide study reports which positions differ between people with a condition and people without, at the population level, and that is all this page repeats. A question about a symptom, a test or a treatment belongs with a clinician.
Databases, guidelines and references
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Nephrotic Syndrome, Type 4. MyGeneLog™. https://www.mygenelog.com/conditions/nephrotic-syndrome-type-4
Nephrotic Syndrome, Type 4 is the condition the GWAS Catalog files under "Nephrotic syndrome, type 4". This page does not define it in its own words; it lists what genome-wide studies have reported: 14 positions from 1 study, with each study's sample and citation.
Genome-wide studies have reported 14 associated positions. Each common variant has a small effect, and an association in a population is not a cause in any one person.
The catalogue maps the positions to 2 genes: WT1, LOC107982234. These are where the positions sit, not proof of how they act.
No. They are population-level findings of small effect. Nephrotic Syndrome, Type 4 is diagnosed by a clinician, and no guideline uses a genotype to predict it.
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