Research
Tag

Sleep

69 genetic variants with this tag.

RSID Gene Description Category
rs10462020 PER3 V647G Missense variant in circadian clock gene PER3 associated with morning chronot... Hormones & Sleep Moderate
rs10038916 GRIA1 Intronic variant in the AMPA glutamate receptor gene GRIA1 associated with re... Neurology & Cognition Strong
rs1064608 MTCH2 Pro290Ala Missense variant in MTCH2 that reduces mitochondrial metabolic efficiency, in... Hormones & Sleep Moderate
rs10766383 NUCB2 Intronic NUCB2 variant associated with type 2 diabetes risk in females and or... Hormones & Sleep Moderate
rs10830963 MTNR1B Intron C>G Melatonin receptor variant that extends nighttime melatonin signaling in panc... Hormones & Sleep Established
rs10947690 MDGA1 Leu61Pro Missense variant in the inhibitory synapse regulator MDGA1 that impairs neuro... Hormones & Sleep Strong
rs11071559 RORA Intronic variant in the circadian clock regulator RORA; the T allele is prote... Allergy & Atopic Disease Moderate
rs1144566 RGS16 RGS16 H137R Missense variant in RGS16 that substitutes histidine for arginine at position... Hormones & Sleep Moderate
rs1154155 TRA T-cell receptor alpha locus variant associated with narcolepsy susceptibility... Hormones & Sleep Strong
rs10839553 CCKBR Intronic variant near the cholecystokinin B receptor gene associated with res... Neurology & Cognition Strong
rs11545787 RASD1 RASD1 photic entrainment variant 3' UTR variant in RASD1 (Dexras1), a GTPase that gates light signals to the c... Hormones & Sleep Strong
rs10895816 GRIA4 Intronic variant in the AMPA glutamate receptor gene GRIA4 associated with re... Neurology & Cognition Strong
rs11605924 CRY2 Intron Variant Circadian clock gene variant affecting fasting glucose, hepatic lipid metabol... Hormones & Sleep Strong
rs12736689 RGS16 Intronic/regulatory variant near RGS16 that is the strongest single-locus mor... Hormones & Sleep Strong
rs1330 NUCB2 Intronic NUCB2 variant associated with obesity risk in males, type 2 diabetes... Hormones & Sleep Moderate
rs117896735 INPP5F Intronic variant in the INPP5F/BAG3 locus associated with increased risk of R... Neurology & Cognition Strong
rs1369481 NPAS2 Intronic variant in the brain-specific circadian transcription factor NPAS2; ... Hormones & Sleep Emerging
rs139315125 PER3 H417R Rare PER3 missense variant that co-occurs on the FASPS3 haplotype with Pro415... Hormones & Sleep Strong
rs57875989 PER3 PER3 VNTR (4/5 repeat) Coding VNTR in exon 18 of the circadian clock gene PER3; 4-repeat vs 5-repeat... Arrhythmia & Heart Rhythm Moderate
rs150812083 PER3 PER3 Pro415Ala (FASPS3) Rare PER3 missense variant that destabilizes the circadian clock protein, sho... Hormones & Sleep Strong
rs1554483 CLOCK Intronic CLOCK variant whose G allele, in a haplotype with rs4864548 A, confe... Hormones & Sleep Moderate
rs17493811 AGER Tag SNP in the AGER 3′ downstream region associated with increased type 1 dia... Hormones & Sleep Moderate
rs17679445 PNPO Arg116Gln Missense variant in pyridoxamine 5'-phosphate oxidase that reduces the enzyme... Hormones & Sleep Moderate
rs2271933 HCRTR1 Ile408Val Missense variant in the orexin/hypocretin receptor 1 that alters G-protein si... Mood & Behavior Moderate
rs12693542 SLC40A1 Regulatory variant upstream of ferroportin (the sole cellular iron exporter) ... Neurology & Cognition Strong
rs12752133 GBA Intronic GBA variant associated with REM sleep behavior disorder via lysosoma... Neurology & Cognition Strong
rs1800624 AGER -374T/A Promoter variant in the AGER gene that increases RAGE transcription approxima... Hormones & Sleep Moderate
rs1801260 CLOCK 3111T>C (3'UTR) Core circadian clock transcription factor variant affecting mRNA stability, a... Hormones & Sleep Moderate
rs184039278 CRY1 CRY1Δ11 Splice-site variant in the circadian clock gene CRY1 that causes exon 11 skip... Hormones & Sleep Strong
rs1991517 TSHR Asp727Glu Affects TSH receptor sensitivity and thyroid hormone regulation; influences T... Hormones & Sleep Strong
rs1562444 MTNR1B MTNR1B 3'UTR Melatonin Signaling Variant Regulatory 3'UTR variant in the melatonin receptor 1B gene that affects MTNR1... Blood Sugar & Diabetes Moderate
rs2050122 HTR6 Regulatory variant near the HTR6 serotonin 6 receptor gene associated with ch... Hormones & Sleep Moderate
rs2066853 AHR Arg554Lys Aryl hydrocarbon receptor variant in the transactivation domain that alters A... Hormones & Sleep Moderate
rs2070600 AGER Gly82Ser Missense variant in the AGER pattern-recognition receptor that reduces solubl... Hormones & Sleep Strong
rs228697 PER3 Pro864Ala Core clock gene variant that shifts circadian period length and influences mo... Hormones & Sleep Moderate
rs2287161 CRY1 3' Downstream G>C Cryptochrome 1 circadian gene variant influencing glucose metabolism, sleep t... Hormones & Sleep Strong
rs2291725 GIP Ser103Gly Missense variant in the GIP incretin hormone that changes its bioactivity and... Hormones & Sleep Moderate
rs2304672 PER2 5'UTR C111G Regulatory variant in a core clock gene that influences circadian timing, sle... Hormones & Sleep Moderate
rs2325751 PNPO Regulatory variant 2 kb upstream of PNPO that may alter expression of the vit... Hormones & Sleep Emerging
rs2675703 OPN4 Missense variant (Pro10Leu) in melanopsin, the photopigment driving circadian... Hormones & Sleep Emerging
rs28362944 SERPING1 5' UTR variant in C1-inhibitor gene that promotes partial exon 2 skipping, re... Hormones & Sleep Moderate
rs324981 NPSR1 Asn107Ile Gain-of-function missense variant in the neuropeptide S receptor that increas... Hormones & Sleep Moderate
rs2230912 P2RX7 Gln460Arg Missense variant in the C-terminal domain of the P2X7 receptor that disrupts ... Neurology & Cognition Moderate
rs34714364 APH1A APH1A gamma-secretase variant Synonymous variant in CA14 near APH1A; T allele is associated with morning ch... Hormones & Sleep Moderate
rs34903499 VIP Synonymous coding variant in the VIP gene (Asn133Asn); the T allele may alter... Hormones & Sleep Emerging
rs35333999 PER2 V903I Missense variant in core circadian clock gene PER2 that lengthens intrinsic c... Hormones & Sleep Strong
rs35833281 HCRTR2 Intronic variant in the orexin/hypocretin receptor 2 gene that tags the HCRTR... Hormones & Sleep Strong
rs3754048 APH1A -980C/G Regulatory variant 2 kb upstream of APH1A where the C allele (paper's G, codi... Hormones & Sleep Moderate
rs3816183 HAAO Ile37Val Missense variant in the kynurenine pathway enzyme HAAO that shifts tryptophan... Hormones & Sleep Moderate
rs3923809 BTBD9 Second independent intronic BTBD9 variant associated with restless legs syndr... Hormones & Sleep Strong
rs2653349 HCRTR2 Ile308Val Missense variant at position 308 of the orexin receptor 2 protein; the minor ... Neurology & Cognition Strong
rs4307059 CDH9/CDH10 Intergenic variant at 5p14.1 between neuronal cell-adhesion genes CDH9 and CD... Hormones & Sleep Strong
rs4410790 AHR Regulatory variant 54 kb upstream of the aryl hydrocarbon receptor gene; the ... Hormones & Sleep Strong
rs306960 PTK2 Intronic variant in PTK2 (focal adhesion kinase) linked to restless legs synd... Neurology & Cognition Strong
rs4446909 ASMT Promoter A>G Final enzyme in melatonin synthesis; promoter variant reduces ASMT expression... Hormones & Sleep Moderate
rs3129934 HLA-DRB5 DR15 haplotype tag Tag SNP for HLA-DRB5*01:01 on the DR15 susceptibility haplotype, physically n... Neurology & Cognition Strong
rs4746 GLO1 Glu111Ala Missense variant in glyoxalase 1 reducing enzyme activity, allowing methylgly... Hormones & Sleep Moderate
rs4753426 MTNR1B Promoter variant in the melatonin receptor 1B gene that alters MTNR1B express... Hormones & Sleep Moderate
rs4926 SERPING1 Val480Met Missense variant in C1-inhibitor gene associated with insomnia risk through n... Hormones & Sleep Moderate
rs516134 RGS16 RGS16 chronotype variant Regulatory variant ~20 kb downstream of RGS16 that influences circadian chron... Hormones & Sleep Strong
rs55694368 PER2 PER2 regulatory variant Upstream regulatory signal near the core circadian clock gene PER2 that shift... Hormones & Sleep Strong
rs5751876 ADORA2A 1976T>C Adenosine A2A receptor variant that determines individual sensitivity to caff... Hormones & Sleep Strong
rs3756059 SNCA Intronic SNCA variant at the 5′ locus associated with REM sleep behavior diso... Neurology & Cognition Strong
rs757081 NUCB2 Gln338Glu (Q338E) Missense variant in nucleobindin-2, the precursor protein cleaved to produce ... Hormones & Sleep Moderate
rs9394502 BTBD9 BTBD9 insomnia/RLS variant Intronic variant in the canonical restless legs syndrome gene BTBD9, associat... Hormones & Sleep Strong
rs9479402 VIP VIP chronotype variant Intergenic variant ~54 kb downstream of the VIP gene; the C allele reduces VI... Hormones & Sleep Strong
rs9565309 FBXL3 FBXL3 circadian variant Regulatory variant near FBXL3 that modulates circadian period length; the C a... Hormones & Sleep Strong
rs76763715 GBA N409S GBA missense variant (p.Asn409Ser, formerly N370S) — the most common GBA path... Neurology & Cognition Established
rs7697073 SCARB2 Intronic SCARB2 variant associated with REM sleep behavior disorder risk via ... Neurology & Cognition Moderate