Gene Knowledge Graph
UTC

All variants

Continuously updated · newest added Sep 16, 2026

12,481 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
Standard on its own

Growth differentiation factor-15 levels

PGPEP1 · rs1054564

See detailed info → Standard on its own

Growth differentiation factor-15 levels

PGPEP1 · rs888663

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

Immune reponse to smallpox (secreted IL-1beta)

LOC389936 · rs12247397

See detailed info → Sensitive

Coronary heart disease

SMG6 · rs1231206

See detailed info → Sensitive

Breast cancer

ESR1 · rs2046210

See detailed info → Standard on its own

Vitamin E levels

SCARB1 · rs11057830

See detailed info → Standard

HDL cholesterol

ABCA1 · rs3905000

See detailed info → Standard on its own

HPV seropositivity

HLA-DQB1 · rs9357152

See detailed info → Standard

Pulmonary function

ARMC2 · rs2798641

See detailed info → Standard

Pulmonary function

MMP15 · rs12447804

See detailed info → Standard

Pulmonary function

ZKSCAN3 · rs6903823

See detailed info → Sensitive

Bipolar disorder

CANCNA1C · rs4765913

See detailed info → Sensitive

Polycystic ovary syndrome

ZFP36L2 · rs12478601

See detailed info → Standard

Body mass index

MTCH2 · rs10838738

See detailed info → Standard

Cholesterol, total

APOB · rs693

See detailed info → Standard

Blood pressure

SLC4A7 · rs13082711

See detailed info → Standard

Hepatitis B

GRIN2A · rs11866328

See detailed info →

Showing 20 of 12481 · page 562 of 625

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.