Gene Knowledge Graph
UTC

All variants

Continuously updated · newest added Oct 26, 2026

137,364 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 Strongest evidence

Strength of the evidence: all 2+ 3+ 4

Standard

Total cholesterol levels

G6PD · rs762517

See detailed info → Standard

Glycated hemoglobin levels

G6PD · rs72554664

See detailed info → Standard

Hemoglobin levels

G6PD · rs5030868

See detailed info → Sensitive

Systemic lupus erythematosus

G6PD · rs5945199

See detailed info → Sensitive

G6PD deficiency (G6PD A+ / A- component)

G6PD · rs1050829

See detailed info → Sensitive

G6PD deficiency (G6PD A-)

G6PD · rs1050828

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.