Variants linked to Neuroticism

Continuously updated · newest added Oct 25, 2026

301 positions on this site are linked to Neuroticism, out of 118,462 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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General factor of neuroticism

ZDHHC20P4 · rs9541684

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Neuroticism

TMEM106B · rs57506017

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Neuroticism (MTAG)

PROX2 · rs2359239

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General factor of neuroticism

ENSG00000239065 · rs12680442

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Neuroticism

XKR6 · rs2409722

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Neuroticism

TYR · rs10830244

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Neuroticism

near TLR4 · rs7034482

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General factor of neuroticism

DRD2 · rs7927693

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General factor of neuroticism

ENSG00000270966 · rs406123

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General factor of neuroticism

MAPT · rs2435200

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General factor of neuroticism

SGK223 · rs17603933

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General factor of neuroticism

ENSG00000243516 · rs1559903

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General factor of neuroticism

ZDHHC20P4 · rs8002150

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General factor of neuroticism in mitochondrial haplogroup X

near NACC2 · rs72771986

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Neuroticism

LINC02210-CRHR1 · rs12944712

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General factor of neuroticism

RP11-105N13.4 · rs11650571

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General factor of neuroticism

MSRA · rs10089263

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Neuroticism

near SUDS3 · rs56080343

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General factor of neuroticism

PCDH9 · rs147861665

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Neuroticism

ZNF184 · rs113039233

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Showing 20 of 301 · page 3 of 16

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.