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 103,904 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

near CDCA7 · rs74527054

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Standard

Male-pattern baldness

CDYL2 · rs74794145

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Standard

Male-pattern baldness

ZNF462 · rs73667301

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Standard

Male-pattern baldness

SLC1A3 · rs75096272

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Standard

Male-pattern baldness

near ATP11B · rs74614808

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Standard

Male-pattern baldness

near FOXF2 · rs75294181

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Standard

Male-pattern baldness

SLC14A2 · rs74951270

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Standard

Male-pattern baldness

MVB12B · rs73668018

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Standard

Male-pattern baldness

near TFAP2A · rs72834043

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Standard

Male-pattern baldness

SLC14A2 · rs72906315

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Standard

Male-pattern baldness

near KRT25 · rs72821884

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Standard

Male-pattern baldness

PEPD · rs73030120

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Standard

Male-pattern baldness

near MYOCD · rs72809176

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Standard

Male-pattern baldness

PRDM1 · rs72941618

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Standard

Male-pattern baldness

near HSPA4 · rs72801474

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Standard

Male-pattern baldness

ATF7IP · rs7313259

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Standard

Male-pattern baldness

PRDM6 · rs72787559

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Standard

Male-pattern baldness

near UTP25 · rs724286

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Standard

Male-pattern baldness

TBX15 · rs72705338

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Standard

Male-pattern baldness

near AXIN2 · rs7222794

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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.