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

near CNTLN · rs263645

See detailed info → Sensitive

Depression

LINC03051 · rs6783233

See detailed info → Sensitive

Depression

near KLF7 · rs62188629

See detailed info → Sensitive

Depression

near BRINP2 · rs72710803

See detailed info → Sensitive

Depression

FHIT · rs141954845

See detailed info → Sensitive

Depression

CACNA1E · rs169235

See detailed info → Sensitive

Depression

HTT · rs7685686

See detailed info → Sensitive

Depression

ELAVL4 · rs11579246

See detailed info → Sensitive

Depression

near BEND4 · rs34937911

See detailed info → Sensitive

Depression

COP1 · rs10913112

See detailed info → Sensitive

Depression

near GRIK3 · rs1002656

See detailed info → Sensitive

Depression (broad)

near MUC21 · rs3131781

See detailed info → Sensitive

Depression (broad)

near CTTNBP2 · rs2402273

See detailed info → Sensitive

Depression (broad)

GPX6 · rs13191038

See detailed info → Sensitive

Depression (broad)

near ZNF184 · rs35715914

See detailed info → Sensitive

Depression (broad)

near HLA-G · rs9258375

See detailed info → Sensitive

Depression (broad)

near TRIM27 · rs9257248

See detailed info → Sensitive

Depression (broad)

near CNTLN · rs263575

See detailed info → Sensitive

Depression (broad)

KCNQ5 · rs112348907

See detailed info → Sensitive

Depression (broad)

near ZNF311 · rs3129791

See detailed info →

Showing 20 of 99 · page 2 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.