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

HDAC9 · rs10278449

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Standard

Male-pattern baldness

WNT10A · rs74333950

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Standard

Male-pattern baldness

GNL3L · rs140707533

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Standard

Male-pattern baldness

near APCDD1 · rs56335910

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Standard

Male-pattern baldness

HMGB1 · rs9578178

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Standard

Male-pattern baldness

near KREMEN2 · rs986358

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Standard

Male-pattern baldness

COL4A2 · rs9559793

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Standard

Male-pattern baldness

near DLX4 · rs9896363

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Standard

Male-pattern baldness

CIC · rs9636121

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Standard

Male-pattern baldness

near BAHCC1 · rs9898002

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Standard

Male-pattern baldness

near GPR132 · rs56256371

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Standard

Male-pattern baldness

near ETAA1 · rs56225803

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Standard

Male-pattern baldness

near TWIST2 · rs56116740

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Standard

Male-pattern baldness

near MYOCD · rs4792260

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Standard

Male-pattern baldness

PARVA · rs4757420

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Standard

Male-pattern baldness

near TMEM270 · rs4717827

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Standard

Male-pattern baldness

EXT2 · rs4551754

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Standard

Male-pattern baldness

near DLL1 · rs4710758

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Standard

Male-pattern baldness

PRDM6 · rs509256

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Standard

Male-pattern baldness

HEXIM2 · rs4792819

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Showing 20 of 337 · page 5 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.