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

LGR4 · rs2169849

See detailed info →
Standard

Male-pattern baldness

near FOXP4 · rs2477826

See detailed info →
Standard

Male-pattern baldness

TBX15 · rs2489245

See detailed info →
Standard

Male-pattern baldness

near ASB7 · rs2641224

See detailed info →
Standard

Male-pattern baldness

PRKD1 · rs225847

See detailed info →
Standard

Male-pattern baldness

CTNNB1 · rs2293304

See detailed info →
Standard

Male-pattern baldness

near HAND1 · rs1846967

See detailed info →
Standard

Male-pattern baldness

near CLINT1 · rs182720683

See detailed info →
Standard

Male-pattern baldness

HOXC12 · rs180807105

See detailed info →
Standard

Male-pattern baldness

PAX1 · rs77410716

See detailed info →
Standard

Male-pattern baldness

RSPO2 · rs77767830

See detailed info →
Standard

Male-pattern baldness

RUNX1 · rs68088846

See detailed info →
Standard

Male-pattern baldness

AR · rs7061504

See detailed info →
Standard

Male-pattern baldness

near FZD10 · rs76972608

See detailed info →
Standard

Male-pattern baldness

METTL10 · rs3781452

See detailed info →
Standard

Male-pattern baldness

FAR2 · rs7976269

See detailed info →
Standard

Male-pattern baldness

C10orf11 · rs11593840

See detailed info →
Standard

Male-pattern baldness

MSI2 · rs17833789

See detailed info →
Standard

Male-pattern baldness

AUTS2 · rs4718886

See detailed info →
Standard

Male-pattern baldness

RSPO2 · rs79593277

See detailed info →

Showing 20 of 337 · page 16 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.