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 118,630 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 (MTAG)

BSN · rs2029591

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Sensitive

Major depressive disorder (broad)

MOB4 · rs1563340

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Sensitive

Major depressive disorder or severe COVID-19 (pleiotropy)

MAPT-AS1 · rs1396862

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Sensitive

Major depressive disorder (broad)

MYH15 · rs113689582

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Sensitive

Major depressive disorder (broad)

near Y_RNA · rs2187490

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Sensitive

Major depressive disorder (broad)

LINC02240 · rs13180906

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Sensitive

Major depressive disorder (broad)

near HMGB1P18 · rs12075452

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Sensitive

Major depressive disorder (broad)

SAMD5 · rs9497822

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Sensitive

Major depressive disorder (broad)

LSAMP · rs76954012

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Sensitive

Major depressive disorder or hospitalized COVID-19 (pleiotropy)

NSF · rs199457

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Sensitive

Major depressive disorder (broad)

LINC01507 · rs60172152

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Sensitive

Major depressive disorder (broad)

RAB27B · rs2008551

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Sensitive

Major depressive disorder (broad)

CACNA1E · rs199929

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Sensitive

Bipolar disorder or major depressive disorder

near ACADS · rs58235352

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Sensitive

Major depressive disorder (broad)

MTHFD1 · rs12886138

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Sensitive

Major depressive disorder (broad)

near ADH5P4 · rs9351533

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Sensitive

Major depressive disorder (broad)

IGSF6 · rs3091404

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Sensitive

Major depressive disorder (MTAG)

DCC · rs1367635

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Sensitive

Major depressive disorder (broad)

ARB2A · rs72786643

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Sensitive

Major depressive disorder (broad)

LINC02796 · rs7415357

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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.