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

HEXIM2 · rs4792819

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Standard

Male-pattern baldness

near MYOCD · rs4792260

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Standard

Male-pattern baldness

near RNF217 · rs4896598

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Standard

Male-pattern baldness

PARVA · rs4757420

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Standard

Male-pattern baldness

MAML2 · rs485642

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Standard

Male-pattern baldness

EXT2 · rs4551754

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Standard

Male-pattern baldness

near RUNX3 · rs9438874

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Standard

Male-pattern baldness

ZC3H11A · rs80226387

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Standard

Male-pattern baldness

FYN · rs804193

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Standard

Male-pattern baldness

near HMGB1 · rs9315009

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Standard

Male-pattern baldness

near GTF2A1 · rs8011097

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Standard

Male-pattern baldness

near APCDD1 · rs88943

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Standard

Male-pattern baldness

ATP5MC2 · rs7962971

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Standard

Male-pattern baldness

RORA · rs77951645

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Standard

Male-pattern baldness

EBF1 · rs7736883

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Standard

Male-pattern baldness

GLIS1 · rs761489

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Standard

Male-pattern baldness

MYO3B · rs7562756

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Standard

Male-pattern baldness

near RORB · rs77123275

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Standard

Male-pattern baldness

PBX1 · rs79768173

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Standard

Male-pattern baldness

near SRD5A2 · rs76712439

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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.