Variants linked to Major Depressive Disorder

Continuously updated · newest added Oct 25, 2026

106 positions on this site are linked to Major Depressive Disorder, out of 118,420 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Major Depressive Disorder

Sensitive

Major depressive disorder

near RN7SL618P · rs1867368

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Sensitive

Major depressive disorder (broad)

DENND1A · rs79924686

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Sensitive

Major depressive disorder (MTAG)

ERBB4 · rs72948506

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Sensitive

Major depressive disorder (broad)

HS6ST3 · rs72642767

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Sensitive

Major depressive disorder (broad)

LUZP2 · rs16912792

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Sensitive

Major depressive disorder (broad)

DCDC2 · rs12197973

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Sensitive

Major depressive disorder

near LINC03131 · rs11515172

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Sensitive

Major depressive disorder (MTAG)

near MRPL46 · rs8035777

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Sensitive

Bipolar disorder or major depressive disorder

CACNA1C · rs769087

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Sensitive

Major depressive disorder (MTAG)

FAM120A · rs6479487

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Sensitive

Major depressive disorder (broad)

near MIR4432HG · rs4672382

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Sensitive

Suicide attempts in major depressive disorder

ARL5B · rs45593736

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Sensitive

Major depressive disorder

PALMD · rs3818852

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Sensitive

Major depressive disorder (broad)

BMERB1 · rs170194

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Sensitive

Major depressive disorder (MTAG)

HS6ST3 · rs1414622

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Sensitive

Major depressive disorder

near PURPL · rs12054895

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Sensitive

Major depressive disorder (broad)

near LINC02484 · rs7675024

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Sensitive

Major depressive disorder (broad)

RBMS3 · rs6783423

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Sensitive

Major depressive disorder (broad)

near EVX2 · rs6752623

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Sensitive

Bipolar disorder or major depressive disorder

near PSMC1P5 · rs55993664

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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.