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

APOA1 · rs613808

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Standard

Male-pattern baldness

near CDYL · rs6597081

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Standard

Male-pattern baldness

COL23A1 · rs61739424

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Standard

Male-pattern baldness

near PDGFA · rs62433864

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Standard

Male-pattern baldness

CIROZ · rs6696575

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Standard

Male-pattern baldness

near COL24A1 · rs6674512

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Standard

Male-pattern baldness

SULF2 · rs66806308

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Standard

Male-pattern baldness

KSR2 · rs61640416

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Standard

Male-pattern baldness

ISM1 · rs6041981

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Standard

Male-pattern baldness

near AHCY · rs6088466

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Standard

Male-pattern baldness

near HAPSTR1 · rs59642482

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Standard

Male-pattern baldness

ISM1 · rs17191004

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Standard

Male-pattern baldness

WARS2 · rs17023135

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Standard

Male-pattern baldness

near FOXD2 · rs17379854

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Standard

Male-pattern baldness

EHBP1 · rs17408037

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Standard

Male-pattern baldness

near MTX2 · rs16863925

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Standard

Male-pattern baldness

near PRR9 · rs16835093

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Standard

Male-pattern baldness

near LHX2 · rs16936765

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Standard

Male-pattern baldness

near VAPA · rs17435937

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Standard

Male-pattern baldness

RORA · rs1680446

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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.