Variants linked to Bipolar Disorder

Continuously updated · newest added Oct 23, 2026

95 positions on this site are linked to Bipolar Disorder, out of 111,351 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 Bipolar Disorder

Sensitive

Bipolar disorder (MTAG)

LINC01830 · rs11887562

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Sensitive

Bipolar disorder

FSTL5 · rs11724116

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Sensitive

Bipolar disorder

MDFIC2 · rs115694474

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Sensitive

Bipolar disorder

ZCCHC7 · rs10973201

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Sensitive

Response to lithium treatment in bipolar disorder (continuous phenotype)

AL157359.3 · rs78015114

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Sensitive

Bipolar I disorder

ATP2B2 · rs735931

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Sensitive

Bipolar disorder (MTAG)

MAU2 · rs4239639

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Sensitive

Bipolar disorder (MTAG)

near CCT4P1 · rs13236223

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Sensitive

Bipolar disorder (MTAG)

TMEM56 · rs12563424

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Sensitive

Bipolar disorder (MTAG)

GRIN2A · rs11648559

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Sensitive

Bipolar disorder

SSBP2 · rs6887473

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Sensitive

Response to antiepileptic mood-stabilizing treatment in bipolar disorder

THSD7A · rs78835388

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Sensitive

Bipolar disorder

RPL13 · rs12932628

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Sensitive

Bipolar disorder

ZNF592 · rs12902052

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Sensitive

Bipolar disorder

RP1-84O15.2 (lincRNA) · rs2953928

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Sensitive

Bipolar disorder

VRK2 · rs41335055

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Sensitive

Bipolar disorder

KCNB1 · rs237460

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Sensitive

Bipolar disorder

SLC25A12 · rs75776799

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Sensitive

Bipolar disorder or body mass index

near FTH1P5 · rs4141973

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Sensitive

Bipolar disorder

ADCY2 · rs28565152

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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.