Variants linked to Polycystic Ovary Syndrome

Continuously updated · newest added Oct 25, 2026

26 positions on this site are linked to Polycystic Ovary Syndrome, out of 118,378 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 Polycystic Ovary Syndrome

Sensitive

Polycystic ovary syndrome in overweight/obese individuals (BMI > 25 kg/m2)

DENND1A · rs569675099

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Sensitive

Polycystic ovary syndrome in lean individuals (BMI <= 25 kg/m2)

DENND1A · rs12000707

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Sensitive

Fasting glucose (adjusted for BMI) or polycystic ovary syndrome (pleiotropy)

ADCY5 · rs9844212

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Sensitive

Polycystic ovary syndrome (adjusted for age and BMI)

DENND1A · rs3945628

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Sensitive

Polycystic ovary syndrome (adjusted for age)

ZNFR3 · rs145598156

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Sensitive

Polycystic ovary syndrome (reproductive subtype)

IQCA1 · rs76182733

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Sensitive

Polycystic ovary syndrome

C9orf3 · rs10993397

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Sensitive

Polycystic ovary syndrome

SOD2 · rs17186366

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Sensitive

Polycystic ovary syndrome (reproductive subtype)

KAZN · rs78025940

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Sensitive

Polycystic ovary syndrome (adjusted for age)

ZBTB16 · rs1672716

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Sensitive

Polycystic ovary syndrome

ERBB4 · rs113168128

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Sensitive

Polycystic ovary syndrome (adjusted for age)

FSHB · rs11031002

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Sensitive

Polycystic ovary syndrome (adjusted for age)

ERB4 · rs7564590

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Sensitive

Polycystic ovary syndrome

DENND1A · rs9696009

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Sensitive

Polycystic ovary syndrome

ZBTB16 · rs1784692

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Sensitive

Polycystic ovary syndrome

KRR1 · rs1795379

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Sensitive

Polycystic ovary syndrome

TOX3 · rs8043701

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Sensitive

Polycystic ovary syndrome

FSHB · rs11031006

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Sensitive

Polycystic ovary syndrome

ERBB4 · rs1351592

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Sensitive

Polycystic ovary syndrome

SUMO1P1 · rs6022786

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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.