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 104,072 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

STAU2 · rs11774977

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Standard

Male-pattern baldness

near BHLHE40 · rs11715919

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Standard

Male-pattern baldness

near CDYL2 · rs117538856

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Standard

Male-pattern baldness

near FOXF2 · rs11756214

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Standard

Male-pattern baldness

near KLF12 · rs11619505

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Standard

Male-pattern baldness

near CRYAA · rs115557929

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Standard

Male-pattern baldness

GIN1 · rs115505614

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Standard

Male-pattern baldness

RERE · rs115109046

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Standard

Male-pattern baldness

near BMP7 · rs1150428

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Standard

Male-pattern baldness

BORCS5 · rs11537452

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Standard

Male-pattern baldness

near CCDC91 · rs11049328

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Standard

Male-pattern baldness

CMPK1 · rs11211532

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Standard

Male-pattern baldness

THADA · rs11124931

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Standard

Male-pattern baldness

FYN · rs11153311

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Standard

Male-pattern baldness

near EBF1 · rs112371596

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Standard

Male-pattern baldness

KCNMA1 · rs17480656

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Standard

Male-pattern baldness

NREP · rs17842602

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Standard

Male-pattern baldness

TGFB1 · rs1800472

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Standard

Male-pattern baldness

near DLG5 · rs17516020

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Standard

Male-pattern baldness

LITAF · rs17523630

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Showing 20 of 337 · page 13 of 17

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.