All variants

Continuously updated · newest added Oct 24, 2026

113,994 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.

Standard

BTN2A1 protein levels

near HLA-B · rs3134792

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Standard

GZMB protein levels

HLA-B · rs41563615

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Standard

alpha-2-macroglobulin receptor-associated protein levels (LRPAP1.3640.14.3)

HLA-B · rs41552714

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Standard on its own

Monounsaturated fatty acid levels

near HLA-B · rs2442728

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Standard

Hip circumference adjusted for BMI

HLA-B · rs9378247

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Standard

A body shape index

HLA-B · rs1055890

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Standard

Waist-to-hip ratio adjusted for BMI

HLA-B · rs28752890

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Sensitive

Human papilloma virus 16 positive oropharyngeal cancer

HLA-B · rs9266329

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Standard

Estimated bone mineral density

HLA-B · rs114029601

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Standard

Free cholesterol to total lipids ratio in small VLDL

HLA-B · rs62396280

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Standard on its own

Serum urate levels

near HLA-B · rs9266061

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Standard

Body size at age 10

HLA-B · rs9265968

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Standard on its own

Polyunsaturated fatty acid levels

near HLA-B · rs2844572

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Standard on its own

Platelet-to-lymphocyte ratio

near HLA-B · rs9265902

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Standard

Plateletcrit

HLA-B · rs3819282

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Standard

Transcription initiation factor IIA subunit 2 levels

HLA-B · rs115881826

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Standard

Appendicular lean mass

HLA-B · rs9266244

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Standard on its own

Polyunsaturated fatty acid levels

near HLA-B · rs11962871

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Standard

Neutrophil percentage of white cells

HLA-B · rs2249935

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Standard

Immature platelet fraction

HLA-B · rs9266265

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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.