Insomnia is the difficulty falling or staying asleep, leading to poor sleep quality and daytime fatigue—often triggered by stress, lifestyle, or underlying health conditions. Research shows that variations near genes involved in circadian rhythm regulation and neurotransmission (like ABCC9, PER3, and GRIA2) can influe...
OpenSNP · European · Human
339 of 2,710 SNPs with zeta at 1.717
OpenSNP · African · Human
335 of 2,710 SNPs with zeta at 1.615
OpenSNP · European American · Human
339 of 2,710 SNPs with zeta at 1.608
OpenSNP · European · Human
339 of 2,710 SNPs with zeta at 1.591
OpenSNP · European · Human
173 of 2,710 SNPs with zeta at 1.536
OpenSNP · European · Human
335 of 2,710 SNPs with zeta at 1.530
OpenSNP · European · Human
339 of 2,710 SNPs with zeta at 1.503
Insomnia (EFO_0004698) is a sleep disorder characterized by persistent difficulty in initiating or maintaining sleep, or experiencing non-restorative sleep, leading to impaired...
EFO_0004698
RNA binding fox-1 homolog 1
The Fox-1 family of RNA-binding proteins is evolutionarily conserved, and regulates tissue-specific alternative splicing in metazoa. Fox-1 recognizes a (U)GCAUG stretch in regul...
POLR1H antisense, pseudogene
CUB and Sushi multiple domains 1
Predicted to act upstream of or within several processes, including learning or memory; mammary gland branching involved in pregnancy; and reproductive structure development. Pr...
cell adhesion molecule 2
This gene encodes a member of the synaptic cell adhesion molecule 1 (SynCAM) family which belongs to the immunoglobulin (Ig) superfamily. The encoded protein has three Ig-like d...
protein tyrosine phosphatase receptor type D
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular proce...
