Gene Knowledge Graph
UTC

All variants

Continuously updated · newest added Oct 21, 2026

102,854 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.

Clear
Newest Oldest
Sensitive

Infective connective tissue disorders (PheCode 712)

CFTR · rs548335381

See detailed info → Standard

Triglycerides to Total Lipids in Small HDL percentage

CFTR · rs6977665

See detailed info → Standard

Free Cholesterol to Cholesteryl Esters in Small HDL ratio

CFTR · rs145380885

See detailed info → Sensitive

Barrett's esophagus or Esophageal adenocarcinoma

CFTR · rs17451754

See detailed info → Sensitive

Cystic fibrosis (F508del)

CFTR · rs113993960

See detailed info → Sensitive

Cystic fibrosis (G551D, a gating variant)

CFTR · rs75527207

See detailed info →

Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.