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

near TRMO · rs17346310

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Standard

Male-pattern baldness

near BCL11A · rs17025388

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Standard

Male-pattern baldness

near MN1 · rs17381914

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Standard

Male-pattern baldness

DKK2 · rs17037148

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Standard

Male-pattern baldness

SLC14A2 · rs1381556

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Standard

Male-pattern baldness

ITPR1 · rs13313995

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Standard

Male-pattern baldness

TNFAIP8 · rs1396609

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Standard

Male-pattern baldness

FMN1 · rs150962800

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Standard

Male-pattern baldness

SMAD3 · rs1498507

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Standard

Male-pattern baldness

BABAM2 · rs13409819

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Standard

Male-pattern baldness

PPM1H · rs12825098

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Standard

Male-pattern baldness

near SRD5A2 · rs13027103

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Standard

Male-pattern baldness

ZBTB20 · rs150338507

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Standard

Male-pattern baldness

CBARP · rs150985681

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Standard

Male-pattern baldness

near CMC2 · rs139157021

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Standard

Male-pattern baldness

MBNL1 · rs13093352

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Standard

Male-pattern baldness

near SYF2 · rs12737245

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Standard

Male-pattern baldness

near IRF2BP2 · rs141885537

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Standard

Male-pattern baldness

near CDCA7 · rs13015604

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Standard

Male-pattern baldness

near CUX1 · rs139978687

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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.