Variants linked to Bipolar Disorder

Continuously updated · newest added Oct 23, 2026

95 positions on this site are linked to Bipolar Disorder, out of 111,183 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)

SLC25A17 · rs138321

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Sensitive

Bipolar disorder (MTAG)

near SUFU · rs11191356

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Sensitive

Bipolar I disorder

HTR6 · rs10917509

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Sensitive

Bipolar disorder (MTAG)

near OTUD7B · rs72692857

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Sensitive

Bipolar disorder

ZNF592 · rs748455

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Sensitive

Bipolar disorder

WFDC12 · rs67712855

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Sensitive

Biological Grandparent (maternal): Bipolar Disorder

DDX25 · rs552029205

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Sensitive

Bipolar disorder (MTAG)

GRIN2A · rs9926049

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Sensitive

Bipolar disorder

DOCK2 · rs10866641

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Sensitive

Biological Father: Bipolar Disorder

DIRC3 · rs529892601

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Sensitive

Biological Mother: Bipolar Disorder

SACS · rs185219225

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Sensitive

Biological Mother: Bipolar Disorder

near CNTN5 · rs184489828

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Sensitive

Biological Father: Bipolar Disorder

near DLG5-AS1 · rs184369225

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Sensitive

Biological Grandparent (maternal): Bipolar Disorder

near ANKRD11 · rs77817138

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Sensitive

Biological Father: Bipolar Disorder

MGLL · rs190958890

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Sensitive

Biological Grandparent (paternal): Bipolar Disorder

CCDC60 · rs541650762

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Sensitive

Biological Grandparent (maternal): Bipolar Disorder

near LINC01122 · rs183292232

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Sensitive

Biological Father: Bipolar Disorder

WDPCP · rs948462796

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Sensitive

Bipolar disorder

ITIH1 · rs2336147

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Sensitive

Biological Grandparent (paternal): Bipolar Disorder

near ATP11AUN · rs534919791

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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.