Gene Knowledge Graph
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Variants linked to Depression (Self-Reported Symptoms)

Continuously updated · newest added Nov 6, 2026

99 positions on this site are linked to Depression (Self-Reported Symptoms), out of 2,500,639 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Depression (Self-Reported Symptoms)

Sensitive

Depression

LRFN5 · rs4904738

See detailed info → Standard

Depressive symptoms

near FAXC · rs9375946

See detailed info → Standard

Depressive symptoms

LPIN3 · rs6072345

See detailed info → Standard

Depressive symptoms

RBFOX1 · rs8063603

See detailed info → Standard

Depressive symptoms

DCC · rs11663393

See detailed info → Standard

Depressive symptoms

DENND1B · rs10922244

See detailed info → Standard

Subjective well-being (MTAG)

ZBTB26 · rs3824535

See detailed info → Standard

Subjective well-being (MTAG)

near SATB1 · rs6787782

See detailed info → Standard

Subjective well-being (MTAG)

RBFOX1 · rs716508

See detailed info → Standard

Subjective well-being (MTAG)

near EMX2 · rs703410

See detailed info → Standard

Subjective well-being (MTAG)

RERE · rs4908768

See detailed info → Standard

Depressive symptoms (MTAG)

DCC · rs8084351

See detailed info → Standard

Subjective well-being (MTAG)

COL19A1 · rs10498870

See detailed info → Standard

Depressive symptoms (MTAG)

KSR2 · rs7134419

See detailed info → Standard

Subjective well-being (MTAG)

VRK2 · rs2678892

See detailed info → Standard

Subjective well-being (MTAG)

near CELF4 · rs11665070

See detailed info → Standard

Depressive symptoms (MTAG)

OPA1 · rs9291059

See detailed info → Standard

Subjective well-being (MTAG)

RAB27B · rs28687557

See detailed info → Standard

Subjective well-being (MTAG)

CSE1L · rs2075679

See detailed info → Standard

Depressive symptoms (MTAG)

near ISL1 · rs62365447

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Showing 20 of 99 · page 4 of 5

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.