Variants linked to Depression (Self-Reported Symptoms)

Continuously updated · newest added Oct 27, 2026

99 positions on this site are linked to Depression (Self-Reported Symptoms), out of 500,067 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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

DAGLA · rs198457

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Sensitive

Depression

PAX5 · rs7030813

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Sensitive

Depression

POU5F2 · rs10061069

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Sensitive

Depression

CTTNBP2 · rs7807677

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Sensitive

Depression

MAD1L1 · rs3823624

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Sensitive

Depression

TMEM161B · rs3099439

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Sensitive

Depression (broad)

near SCAND3 · rs13194504

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Sensitive

Depression (broad)

near H2BC11 · rs66975207

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Sensitive

Depression

METTL9 · rs12923444

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Sensitive

Depression

near EP300 · rs5995992

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Sensitive

Depression

PCDH9 · rs9592461

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Sensitive

Depression

near OLFM4 · rs1343605

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Standard

Depressive symptoms

BLTP1 · rs45510091

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Standard

Depressive symptoms (MTAG)

RERE · rs301806

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Standard

Depressive symptoms (MTAG)

SOX6 · rs2014408

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Sensitive

Depression

TCF4 · rs12967143

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Standard

Subjective well-being (MTAG)

near RNU6-1296P · rs17820772

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Standard

Depressive symptoms (MTAG)

near FAM149B1P1 · rs9944275

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Standard

Subjective well-being

LINC01470 · rs6579956

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Sensitive

Depression

DENND1A · rs2670139

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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.