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 104,240 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

GFOD2 · rs12927959

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Standard

Male-pattern baldness

near SIM1 · rs13209911

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Standard

Male-pattern baldness

NDUFAF6 · rs13257021

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Standard

Male-pattern baldness

near SETBP1 · rs1450807

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Standard

Male-pattern baldness

CASZ1 · rs143353512

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Standard

Male-pattern baldness

ZNF549 · rs1548476

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Standard

Male-pattern baldness

MRPS22 · rs13087765

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Standard

Male-pattern baldness

HDAC4 · rs13010577

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Standard

Male-pattern baldness

near CBFB · rs118064296

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Standard

Male-pattern baldness

near SPAG17 · rs12083887

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Standard

Male-pattern baldness

near SPAG17 · rs12127821

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Standard

Male-pattern baldness

CRYBG2 · rs12059495

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Standard

Male-pattern baldness

near RUNX3 · rs12070150

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Standard

Male-pattern baldness

SLC37A3 · rs12538711

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Standard

Male-pattern baldness

near EFEMP1 · rs11888023

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Standard

Male-pattern baldness

ARHGAP15 · rs12614491

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Standard

Male-pattern baldness

near GSDMC · rs11785932

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Standard

Male-pattern baldness

BCL2 · rs117997962

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Standard

Male-pattern baldness

KREMEN1 · rs12157998

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Standard

Male-pattern baldness

near ALX4 · rs117802187

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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.