Variants linked to Androgenetic Alopecia (Male Pattern Baldness)

Continuously updated · newest added Oct 21, 2026

337 positions on this site are linked to Androgenetic Alopecia (Male Pattern Baldness), out of 103,694 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Androgenetic Alopecia (Male Pattern Baldness)

Standard

Male-pattern baldness

near KLF15 · rs76358556

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Standard

Male-pattern baldness

ZBTB20 · rs78705757

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Standard

Male-pattern baldness

DKK2 · rs76067940

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Standard

Male-pattern baldness

near MBL2 · rs7905367

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Standard

Male-pattern baldness

near SRD5A2 · rs76712439

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Standard

Male-pattern baldness

LRMDA · rs7898528

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Standard

Male-pattern baldness

near KDM7A · rs75511207

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Standard

Male-pattern baldness

PTPN14 · rs79225222

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Standard

Male-pattern baldness

near TNRC6C · rs78057054

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Standard

Male-pattern baldness

EBF1 · rs7710925

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Standard

Male-pattern baldness

RSPO2 · rs7841949

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Standard

Male-pattern baldness

near PTPRC · rs7538393

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Standard

Male-pattern baldness

PBX1 · rs79768173

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Standard

Male-pattern baldness

near RORB · rs77123275

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Standard

Male-pattern baldness

SUPT3H · rs755

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Standard

Male-pattern baldness

ATP5MC2 · rs7962971

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Standard

Male-pattern baldness

BCAR3 · rs79117505

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Standard

Male-pattern baldness

near TMEM131L · rs7687559

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Standard

Male-pattern baldness

near FOXF2 · rs75294181

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Standard

Male-pattern baldness

THADA · rs75126888

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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.