Gene Knowledge Graph
UTC

All variants

Continuously updated · newest added Sep 13, 2026

8,177 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.

Newest Oldest
Sensitive

Bipolar disorder

ANK3 · rs4948418

See detailed info → Standard

Permanent tooth development

HMGA2 · rs12424086

See detailed info → Standard on its own

Testosterone levels

SHBG · rs12150660

See detailed info → Standard

Diisocyanate-induced asthma

ODZ3 · rs908084

See detailed info → Standard on its own

Plasma thyroid-stimulating hormone levels

PDE10A · rs2983511

See detailed info → Sensitive

Renal function and chronic kidney disease

SHROOM3 · rs17319721

See detailed info → Standard on its own

N-glycan levels

FUT8 · rs10483776

See detailed info → Standard on its own

Hypothyroidism

HLA-C · rs2517532

See detailed info → Standard

HDL cholesterol

C6orf106 · rs2814944

See detailed info → Standard

Cholesterol, total

FRK · rs9488822

See detailed info → Standard

Platelet count

HLA-DOA · rs399604

See detailed info → Standard

Cholesterol, total

TMEM57 · rs12027135

See detailed info → Standard

HDL cholesterol

MC4R · rs12967135

See detailed info → Standard

HDL cholesterol

DOCK6 · rs737337

See detailed info → Standard on its own

Growth differentiation factor-15 levels

PGPEP1 · rs888663

See detailed info → Standard on its own

Growth differentiation factor-15 levels

PGPEP1 · rs1054564

See detailed info → Sensitive

Breast cancer

TERT · rs10069690

See detailed info → Standard on its own

Liver enzyme levels (alanine transaminase)

HSD17B13 · rs6834314

See detailed info → Standard on its own

Liver enzyme levels (alanine transaminase)

TRIB1 · rs2954021

See detailed info → Standard on its own

Liver enzyme levels (alkaline phosphatase)

ALPL · rs1976403

See detailed info →

Showing 20 of 8177 · page 346 of 409

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.