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

EIF3E · rs34657911

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Standard

Male-pattern baldness

near MSN · rs5965019

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Standard

Male-pattern baldness

near RUNX3 · rs115176171

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Standard

Male-pattern baldness

near SUCNR1 · rs7648585

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Standard

Male-pattern baldness

near RUNX3 · rs186127900

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Standard

Male-pattern baldness

near EHD3 · rs77781418

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Standard

Male-pattern baldness

TWIST2 · rs146095395

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Standard

Male-pattern baldness

near C1D · rs6756875

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Standard

Male-pattern baldness

near MYOCD · rs72809169

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Standard

Male-pattern baldness

near MSN · rs138876904

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Standard

Male-pattern baldness

near PREP · rs9398035

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Standard

Male-pattern baldness

ZC4H2 · rs6624142

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Standard

Male-pattern baldness

EIF3E · rs118013985

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Standard

Male-pattern baldness

near AR · rs142169094

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Standard

Male-pattern baldness

near NTMT2 · rs71635652

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Standard

Male-pattern baldness

near AR · rs73227823

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Standard

Male-pattern baldness

SPAG17 · rs67803788

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Standard

Male-pattern baldness

ARHGEF9 · rs111810219

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Standard

Male-pattern baldness

HDAC9 · rs10278449

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Standard

Male-pattern baldness

EDA2R · rs79798752

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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.