Variants linked to Sleep and Circadian Rhythm

Continuously updated · newest added Oct 25, 2026

151 positions on this site are linked to Sleep and Circadian Rhythm, out of 118,864 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 Sleep and Circadian Rhythm

Sensitive

Circadian rhythm sleep disorder (PheCode 327.6)

LINC00358 · rs77274901

See detailed info →
Sensitive

Circadian rhythm sleep disorder (PheCode 327.6)

OR2F1 · rs551140100

See detailed info →
Sensitive

Circadian rhythm sleep disorder (PheCode 327.6)

LINC02755 · rs539540831

See detailed info →
Sensitive

Circadian rhythm sleep disorder (PheCode 327.6)

CNTN5 · rs535929585

See detailed info →
Standard

Chronotype

UNC5D · rs6468316

See detailed info →
Standard

Sleep duration

near COX6A1P4 · rs12791153

See detailed info →
Standard

Sleep duration

near LINC02531 · rs9345234

See detailed info →
Standard

Sleep duration

LMAN2 · rs151014368

See detailed info →
Standard

Chronotype

MSI2 · rs8072058

See detailed info →
Standard

Chronotype

R3HDM1 · rs77248969

See detailed info →
Standard

Sleep duration

near FXNP1 · rs11621908

See detailed info →
Standard

Sleep duration

LINC01911 · rs4128364

See detailed info →
Standard

Sleep duration

SCN1A · rs11885663

See detailed info →
Standard

Chronotype

DNAJC12 · rs17712705

See detailed info →
Standard

Sleep duration

NOVA1 · rs6575005

See detailed info →
Standard

Chronotype

ZAK · rs13004345

See detailed info →
Standard

Sleep duration

ERC2 · rs112230981

See detailed info →
Standard

Chronotype

EHMT2 · rs486416

See detailed info →
Standard

Sleep duration

near LINC01377 · rs460692

See detailed info →
Standard

Chronotype

ETNK1 · rs2433634

See detailed info →

Showing 20 of 151 · page 1 of 8

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.