Gene Knowledge Graph
UTC

All variants

Continuously updated · newest added Sep 13, 2026

8,122 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.

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Standard

Body mass index and HDL-C (pairwise)

ARL15 · rs3776717

See detailed info → Standard

Body mass index and HDL-C (pairwise)

ETV5 · rs4234589

See detailed info → Standard on its own

Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test)

SLC30A10 · rs2820443

See detailed info → Standard on its own

Airflow obstruction

AGPHD1 · rs8031948

See detailed info → Standard on its own

Serum ceruloplasmin levels

CP · rs13072552

See detailed info → Standard

Chronic lymphocytic leukemia

ACOXL · rs13401811

See detailed info → Standard on its own

Sunburns

TYR · rs1126809

See detailed info → Standard on its own

Neuritic plaque

GALNT7 · rs62341097

See detailed info → Sensitive

Dementia and core Alzheimer's disease neuropathologic changes

PVRL2 · rs6857

See detailed info → Standard on its own

Toenail selenium levels

BHMT · rs7700970

See detailed info → Sensitive

Cerebrospinal fluid levels of Alzheimer's disease-related proteins

IL6R · rs61812598

See detailed info → Standard on its own

Blood and toenail selenium levels

CBS · rs6586282

See detailed info → Standard on its own

Blood and toenail selenium levels

HOMER1 · rs6859667

See detailed info → Standard on its own

Toenail selenium levels

ARSB · rs17823744

See detailed info → Standard on its own

Mammographic density (dense area)

AREG · rs12642133

See detailed info → Sensitive

Rheumatoid arthritis

ZNF438 · rs793108

See detailed info → Standard on its own

Febrile seizures (MMR vaccine-unrelated)

ANO3 · rs114444506

See detailed info → Standard

Triglycerides

LOC286083 · rs28680850

See detailed info → Sensitive

Rheumatoid arthritis

SFTPD · rs726288

See detailed info → Sensitive

Rheumatoid arthritis

PVT1 · rs1516971

See detailed info →

Showing 20 of 8122 · page 299 of 407

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.