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Bartter Syndrome, as genome-wide studies have reported it: 15 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.
1 study in the GWAS Catalog report 15 positions for Bartter Syndrome, which the catalogue files as "Bartter syndrome". MyGeneLog follows the condition as positions arrive: code builds this page from the records, adds each new position when it is reported, and writes no sentence of its own beyond them.
A study. It contributes 15 positions: rs1007109925 (BSND), rs1301110174 (BSND), rs1366101480 (SLC12A1), rs1451284628 (SLC12A3), rs1644394677 (BSND), rs201540273 (CLCNKB), rs2041199779 (SLC12A1), rs2042079691 (SLC12A1), and 7 more.
The catalogue maps the 15 positions to 5 genes: BSND, SLC12A1, SLC12A3, CLCNKB, KCNJ1. 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 Bartter Syndrome, 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.
A genotype does not diagnose Bartter Syndrome; a clinician does. No guideline uses the 15 variants on this page to predict it, screen for it or confirm it.
Its sources are association records, and association records carry no clinical guidance, so neither does this page. What a genome-wide study reports is a difference between groups of people, not a finding about any one person. Symptoms, tests and treatment are questions for a clinician.
Databases, guidelines and references
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Bartter Syndrome. MyGeneLog™. https://www.mygenelog.com/conditions/bartter-syndrome
Bartter Syndrome is the condition the GWAS Catalog files under "Bartter syndrome". This page does not define it in its own words; it lists what genome-wide studies have reported: 15 positions from 1 study, with each study's sample and citation.
Genes play a part: 15 positions have been linked to it. But each is a common variant of small effect, and a link found across a population does not cause the condition in any one person.
The positions lie in or near 5 genes: BSND, SLC12A1, SLC12A3, CLCNKB, KCNJ1. A mapped gene is the catalogue's location for a position, not a mechanism.
No. They are population-level findings of small effect. Bartter Syndrome is diagnosed by a clinician, and no guideline uses a genotype to predict it.
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