Variants linked to Endometriosis and Depression: Shared Genetics

Continuously updated · newest added Sep 29, 2026

24 positions on this site are linked to Endometriosis and Depression: Shared Genetics, out of 19,838 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 Endometriosis and Depression: Shared Genetics

Standard

Endometriosis

CCDC170 · rs12173791

See detailed info →
Standard

Endometriosis

GREB1 · rs7580473

See detailed info →
Standard

Endometriosis

RNLS · rs4933480

See detailed info →
Standard

Endometriosis

SKAP1 · rs10853098

See detailed info →
Standard

Endometriosis

EEFSEC · rs2999035

See detailed info →
Standard

Endometriosis

near WNT7A · rs2974396

See detailed info →
Standard

Endometriosis

TFPI · rs8176498

See detailed info →
Standard

Endometriosis

IGF1 · rs10860864

See detailed info →
Standard

Endometriosis

CALD1 · rs2290358

See detailed info →
Standard

Endometriosis

near NPVF · rs929240

See detailed info →
Standard

Endometriosis

PAPPA2 · rs10913186

See detailed info →
Standard

Endometriosis

near TSHZ3 · rs384114

See detailed info →
Standard

Endometriosis

ADK · rs10824194

See detailed info →
Sensitive

Endometriosis or depression (pleiotropy)

near COP1 · rs6680839

See detailed info →
Sensitive

Endometriosis or depression (pleiotropy)

DENND1B · rs12118913

See detailed info →
Sensitive

Endometriosis or depression (pleiotropy)

DENND1B · rs2224873

See detailed info →
Sensitive

Endometriosis or depression (pleiotropy)

USP4 · rs6778080

See detailed info →
Sensitive

Endometriosis or depression (pleiotropy)

IP6K1 · rs9835157

See detailed info →
Sensitive

Endometriosis or depression (pleiotropy)

near GRIK3 · rs1395455

See detailed info →
Sensitive

Endometriosis or depression (pleiotropy)

TYR · rs7358418

See detailed info →

Showing 20 of 24 · page 1 of 2

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.