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 103,526 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

BIRC6 · rs72787520

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Standard

Male-pattern baldness

ST3GAL4 · rs11220486

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Standard

Male-pattern baldness

PTHLH · rs11049231

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Standard

Male-pattern baldness

TMEM74 · rs183207557

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Standard

Male-pattern baldness

OPHN1 · rs73212868

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Standard

Male-pattern baldness

TCF4 · rs78803556

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Standard

Male-pattern baldness

TWIST1 · rs73071393

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Standard

Male-pattern baldness

SRD5A2 · rs9282858

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Standard

Male-pattern baldness

BIRC6 · rs72787555

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Standard

Male-pattern baldness

FAR2 · rs74895226

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Standard

Male-pattern baldness

AUTS2 · rs1474368

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Standard

Male-pattern baldness

near CRYAA · rs75732647

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Standard

Male-pattern baldness

TMEM74 · rs77096234

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Standard

Male-pattern baldness

near RHOBTB1 · rs1906457

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Standard

Male-pattern baldness

OPHN1 · rs17302236

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Standard

Male-pattern baldness

near TMEM74 · rs79437808

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Standard

Male-pattern baldness

OPHN1 · rs140488081

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Standard

Male-pattern baldness

VSIG4 · rs147154263

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Standard

Male-pattern baldness

near PAX1 · rs2180439

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Standard

Male-pattern baldness

EBF1 · rs929626

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Showing 20 of 337 · page 1 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.