Why this topic Everyone is wearing a sleep tracker and arguing with it.
2026-04-01 · Portas L, et al., Nature Communications 2026, PMID:41922918
Genetic architecture of sleep in a genome wide association study of device measured sleep traits
Most sleep genetics rests on what people report about their own sleep. This study measured it instead: sleep duration, sleep efficiency, and accelerometer-derived REM and non-REM sleep in 80,013 UK Biobank participants. It found 20 loci, 12 of them not reported before, including genome-wide significant associations for REM and non-REM sleep duration. MEIS1 showed strong opposing effects on REM and non-REM duration. Analysing women and men separately found distinct loci — FOXP2 and NRXN3 in women; LRP1B, NPBWR2 and PABPC4 in men — and Mendelian randomisation supported a link between shorter sleep and higher cardiometabolic risk. The study's MEIS1 position is not in this catalogue; four of its other positions are, including rs2006810 (AUTS2, sleep efficiency) and rs62033400 (FTO, REM sleep duration), which is filed here under body mass index. PMID:41922918.
2026-05-22 · Sinnott-Armstrong N, et al., Nature Communications 2026, PMID:42173832
Genetic variants affect diurnal glucose levels throughout the day
Using the time of day each blood sample was taken in about 420,000 UK Biobank participants, with replication in four other biobanks, the study shows glucose levels are under diurnal genetic control. The two robust time-dependent signals are at MTNR1B, the melatonin receptor, and CRY2, a core clock gene; both independently change type 2 diabetes risk. Those two positions are not on this site yet; 21 others from the study are, including rs560887 (G6PC2) and rs34872471 (TCF7L2).
2026-01-01 · Sleep 2026, PMID:41065713
Insomnia Shares Genetic Risk Loci With Seven Psychiatric Disorders, Largest Study Yet Finds
Genome-wide data from over 314,000 insomnia cases and up to 449,855 cases across 12 psychiatric conditions found significant genetic correlations between insomnia and seven disorders -- ADHD, anorexia nervosa, anxiety, autism spectrum disorder, bipolar disorder, major depressive disorder and schizophrenia -- and 70 shared genomic loci, many novel, converging on GABAergic synapse signaling. This site's own insomnia page covers the underlying genetics in more depth.
Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.
Counted in Europe PMC, where the title or abstract names both this topic and that rsID. The number is papers, not evidence of a cause.
APOE
Lewy body disease
9 papers →BDNF
Smoking behavior
8 papers →FTO
Menarche (age at onset)
7 papers →FTO
Obesity
5 papers →ADCY3
Body mass index
3 papers →MTHFR
Folate metabolism (MTHFR C677T)
3 papers →ABO
Soluble E-selectin levels
3 papers →ALDH2
Alcohol flush reaction
3 papers →CYP1A2
Caffeine metabolism
3 papers →RGS16
Morning vs. evening chronotype
2 papers →OPRM1
Opioid receptor sensitivity
2 papers →PITX2
Atrial fibrillation/atrial flutter
1 paper →CACNA1C
Schizophrenia
1 paper →NRXN3
Waist circumference
1 paper →ARNTL
C-reactive protein levels or triglyceride levels (pleiotropy)
1 paper →RASD1
Morning vs. evening chronotype
1 paper →LPA
Cholesterol, total
1 paper →ADH1B
Alcohol metabolism speed
1 paper →RASD1
Coronary heart disease
1 paper →MC4R
Waist circumference and related phenotypes
1 paper →ADIPOQ
Adiponectin levels
1 paper →PAX8
Sleep duration
1 paper →GPNMB
Parkinson's disease
1 paper →MEIS1
Restless legs syndrome
1 paper →TERT
Lung adenocarcinoma
1 paper →TRIB1
Triglycerides
1 paper →BTBD9
Restless legs syndrome
1 paper →SLCO1B1
Statin muscle-side-effect risk
1 paper →CANCNA1C
Bipolar disorder
1 paper →ABO
Pancreatic cancer
1 paper →EDN1
Circulating vasoactive peptide levels
1 paper →PER2
Morning vs. evening chronotype
1 paper →BDNP
Menarche (age at onset)
1 paper →TAS2R38
Bitter taste perception (PTC/PROP tasting)
1 paper →LRRK2
Parkinson's disease
1 paper →FTO
Type 2 diabetes
1 paper →UGT1A1
Bilirubin levels
1 paper →SLC22A3
Prostate cancer
1 paper →VIP
Morning vs. evening chronotype
1 paper →FBXL3
Morning vs. evening chronotype
1 paper →ZNF259
Triglyceride levels
1 paper →FTO
Obesity (extreme)
1 paper →Europe PMC, title and abstract only, searched for “insomnia”, “sleep duration”, “chronotype”, “circadian preference”, “daytime napping”, “daytime sleepiness”, “sleep apnea” alongside each published rsID. Full text was not counted: it returns every paper with an rsID buried in a supplementary table. Recounted monthly.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Sleep and insomnia. MyGeneLog™. https://www.mygenelog.com/topics/sleep
Sleep and insomnia is this site's topic page for why some people wake at 5am without an alarm and others cannot — tracking which published variants share a paper with sleep-research terms like insomnia, chronotype and sleep apnea.
Partly, for chronotype specifically — some early-rising tendency is inherited — but a variant showing up here is a co-mention, not proof it decided your schedule. Light exposure, work hours, age and stress all shape when someone actually wakes.
Sleep trackers now hand nearly everyone a nightly number, and the question that follows is always whether that number is inherited. This page answers that honestly: a co-mention means a paper discussed sleep and a variant together, not that the variant set the score.
Yes — a missing search term is invisible to this method. The list was widened in 2026 after a check found 38 of the site's variants tied to the trait "Daytime nap" were not being counted because "daytime napping" was not yet a search term.