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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 2,500,080 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)

Standard

Depressive symptoms (MTAG)

NAALADL2 · rs9813064

See detailed info → Standard

Depressive symptoms (MTAG)

near OR5V1 · rs148466862

See detailed info → Standard

Depressive symptoms (MTAG)

NAA11 · rs12642606

See detailed info → Standard

Depressive symptoms (MTAG)

CELF4 · rs4799936

See detailed info → Standard

Depressive symptoms (MTAG)

SEMA6D · rs11855468

See detailed info → Standard

Depressive symptoms (MTAG)

IHO1 · rs4955417

See detailed info → Standard

Depressive symptoms (MTAG)

PSORS1C1 · rs28732100

See detailed info → Standard

Depressive symptoms (MTAG)

MAML3 · rs1877075

See detailed info → Standard

Depressive symptoms (MTAG)

near CCDC68 · rs114658852

See detailed info → Standard

Depressive symptoms (MTAG)

NOS1 · rs1875140

See detailed info → Standard

Depressive symptoms (MTAG)

near CTTNBP2 · rs10244364

See detailed info → Standard

Depressive symptoms (MTAG)

ADGRL4 · rs228568

See detailed info → Standard

Subjective well-being

near ZMYND8 · rs6124977

See detailed info → Standard

Subjective well-being

near SATB1 · rs6769912

See detailed info → Sensitive

Depression

near NEGR1 · rs782212

See detailed info → Standard

Life satisfaction

GATAD2B · rs7554469

See detailed info → Standard

Subjective well-being

RAPGEF6 · rs3756290

See detailed info → Standard

Subjective well-being

NMUR2 · rs4958581

See detailed info → Standard

Subjective well-being

CSE1L · rs2075677

See detailed info →

Showing 19 of 99 · page 5 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.