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

Continuously updated · newest added Nov 8, 2026

99 positions on this site are linked to Depression (Self-Reported Symptoms), out of 2,505,961 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 (broad)

near RPP21 · rs3130116

See detailed info → Sensitive

Depression (broad)

near MUC21 · rs3131781

See detailed info → Sensitive

Depression (broad)

ASTN1 · rs7548151

See detailed info → Sensitive

Depression (broad)

SGIP1 · rs6679379

See detailed info → Sensitive

Depression (broad)

B3GLCT · rs9530139

See detailed info → Sensitive

Depression (broad)

GRM5 · rs6483414

See detailed info → Sensitive

Depression

near CCDC68 · rs12966052

See detailed info → Sensitive

Depression

PIPOX · rs75581564

See detailed info → Sensitive

Depression

STK24 · rs4772087

See detailed info → Sensitive

Depression

near MEIS2 · rs8037355

See detailed info → Sensitive

Depression

SPPL3 · rs3213572

See detailed info → Sensitive

Depression

SHANK2 · rs7117514

See detailed info → Sensitive

Depression

near KIRREL3 · rs57344483

See detailed info → Sensitive

Depression

SORCS3 · rs61867293

See detailed info → Sensitive

Depression

TMEM106B · rs10950398

See detailed info → Sensitive

Depression

RSRC1 · rs7430565

See detailed info → Sensitive

Depression

PMFBP1 · rs11643192

See detailed info → Sensitive

Depression

MIR924HG · rs62099069

See detailed info → Sensitive

Depression

CRYBA1 · rs17727765

See detailed info → Sensitive

Depression

LOC101927421 · rs116755193

See detailed info →

Showing 20 of 99 · page 3 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.