Each page covers one condition properly: what it actually is and what it feels like, what causes it, how common it really is and in whom, and how it's diagnosed — followed by the specific variants with a replicated link to it, and, where the research supports it, how genetics can change the way a medicine behaves.
Written in two registers so one page serves both readers: plain language first, then a clinical detail section with the precise terminology, effect sizes and diagnostic thresholds. Every claim is sourced from freely-available published research and cited on the page, so you can check us — or hand the page to your doctor. 385 conditions so far, growing continuously, and free to reuse with attribution (CC BY 4.0).
Acute Laryngitis and Tracheitis, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 885 cases and 567,247 controls (African American or Afro-Caribbean ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → UrologicalPeyronie's Disease, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 3,199 cases and 571,377 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → UrologicalChronic Renal Failure (CKD), as genome-wide studies have reported it: 2 positions from 1 study, the largest recording 92,642 cases and 521,058 controls (African American or Afro-Caribbean ancestry, Hispanic or Latin American ancestry, East Asian ancestry, European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → UrologicalNephrotic Syndrome without Mention of Glomerulonephritis, as genome-wide studies have reported it: 12 positions from 1 study, the largest recording 1,865 cases and 629,378 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → DigestiveAngiodysplasia of Intestine (without mention of hemorrhage), as genome-wide studies have reported it: 8 positions from 1 study, the largest recording 911 cases and 569,805 controls (African American or Afro-Caribbean ancestry, European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → MusculoskeletalExostosis of Jaw, as genome-wide studies have reported it: 25 positions from 1 study, the largest recording 665 cases and 569,882 controls (African American or Afro-Caribbean ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → AutoimmuneOtosclerosis, as genome-wide studies have reported it: 6 positions from 1 study, the largest recording 3,504 cases and 861,198 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → DigestiveDuodenal Ulcer, as genome-wide studies have reported it: 6 positions from 2 studies, the largest recording 17,117 cases and 867,208 controls (Japanese ancestry, European ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → DigestiveNon-alcoholic Chronic Pancreatitis, as genome-wide studies have reported it: 3 positions from 1 study, the largest recording 584 cases and 6,040 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → CardiovascularCardioembolic Stroke, as genome-wide studies have reported it: 3 positions from 2 studies, the largest recording 10,804 cases and 1,234,808 controls (European ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → OphthalmicAllergic Conjunctivitis, as genome-wide studies have reported it: 4 positions from 1 study, the largest recording 45,734 cases and 1,084,159 controls (European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → DigestiveAcute Pancreatitis, as genome-wide studies have reported it: 6 positions from 3 studies, the largest recording 10,630 cases and 844,679 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → CancerKeratinocyte Cancer, as genome-wide studies have reported it: 4 positions from 1 study, the largest recording 18,538 cases and 340,302 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → ReproductiveAnal and Rectal Polyp, as genome-wide studies have reported it: 6 positions from 1 study, the largest recording 4,766 cases and 607,628 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → CardiovascularBrugada Syndrome, as genome-wide studies have reported it: 7 positions from 2 studies, the largest recording 2,820 cases and 10,001 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → CancerSquamous Cell Carcinoma, as genome-wide studies have reported it: 7 positions from 3 studies, the largest recording 9,674 cases and 625,657 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → RespiratoryChronic Inflammatory Sinonasal Disease, as genome-wide studies have reported it: 2 positions from 1 study, the largest recording 19,901 cases and 199,208 controls. Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → CardiovascularArrhythmia, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 17,861 cases and 194,592 controls (Japanese ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → NeurologicalMeniere's Disease, as genome-wide studies have reported it: 11 positions from 3 studies, the largest recording 8,900 cases and 1,881,340 controls (European ancestry, East Asian ancestry, Hispanic or Latin American ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → AutoimmuneCutaneous Lupus Erythematosus, as genome-wide studies have reported it: 6 positions from 2 studies, the largest recording 1,359 cases and 571,562 controls (African American or Afro-Caribbean ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
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One diagnosed condition or measurable trait covered properly: what it actually is, what causes it, how common it is, how it is diagnosed, and the specific variants with a replicated link to it — every claim sourced from published research.
No. Every page here is informational, not a diagnosis. A result should be discussed with a doctor or a licensed genetic counselor, never acted on alone.
Because they are not disorders. Height, ABO blood group and a handful of others describe a measurable characteristic with nothing to diagnose — "Trait" says so plainly instead of implying a disease that is not one.
Only after a replicated association in published research, verified against the primary study rather than a gene name or a marketing claim — the same discipline the variant pages themselves follow.