Gene Knowledge Graph
UTC

All variants

Continuously updated · newest added Oct 24, 2026

113,826 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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HDL cholesterol levels

HLA-B · rs6902116

See detailed info → Standard

Monocyte count

HLA-B · rs2523562

See detailed info → Standard

Hip circumference adjusted for BMI

HLA-B · rs9266059

See detailed info → Standard

Eosinophil count

near HLA-B · rs2844575

See detailed info → Sensitive

Graves' disease

near HLA-B · rs9265428

See detailed info → Standard

Hypothyroidism

near HLA-B · rs144363644

See detailed info → Standard

Hypothyroidism

near HLA-B · rs73731034

See detailed info → Standard

Lymphocytic thyroiditis

near HLA-B · rs28367766

See detailed info → Standard

Triglycerides to Total Lipids in Large HDL percentage

near HLA-B · rs115168686

See detailed info → Standard

Cholesteryl Esters to Cholesterol in Small VLDL percentage

near HLA-B · rs11968046

See detailed info → Standard

Cholesteryl Esters to Total Lipids in Very Large HDL percentage

near HLA-B · rs36004907

See detailed info → Standard

Free Cholesterol to Total Lipids in Very Large HDL percentage

near HLA-B · rs9265965

See detailed info → Standard

Free Cholesterol to Cholesterol in Very Large HDL percentage

near HLA-B · rs9265568

See detailed info → Standard

HIV setpoint viral load

HLA-B · rs112515516

See detailed info → Standard

Acute anterior uveitis in ankylosing spondylitis

HLA-B · rs115879499

See detailed info → Standard

Takayasu arteritis

HLA-B · rs12524487

See detailed info → Standard

Strep throat

HLA-B · rs1055821

See detailed info → Standard

Neutrophil percentage of white cells

near HLA-B · rs2256752

See detailed info → Standard

Chickenpox

HLA-B · rs9266089

See detailed info → Standard

Lymphocyte count

near HLA-B · rs116438126

See detailed info →

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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.