rs1811399
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | ||
| (T;T) | 0 |
| Make rs1811399(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 100862552 |
| Gene | NPAS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1811399 |
| dbSNP (classic) | rs1811399 |
| ClinGen | rs1811399 |
| ebi | rs1811399 |
| HLI | rs1811399 |
| Exac | rs1811399 |
| Gnomad | rs1811399 |
| Varsome | rs1811399 |
| LitVar | rs1811399 |
| Map | rs1811399 |
| PheGenI | rs1811399 |
| Biobank | rs1811399 |
| 1000 genomes | rs1811399 |
| hgdp | rs1811399 |
| ensembl | rs1811399 |
| geneview | rs1811399 |
| scholar | rs1811399 |
| rs1811399 | |
| pharmgkb | rs1811399 |
| gwascentral | rs1811399 |
| openSNP | rs1811399 |
| 23andMe | rs1811399 |
| SNPshot | rs1811399 |
| SNPdbe | rs1811399 |
| MSV3d | rs1811399 |
| GWAS Ctlg | rs1811399 |
| GMAF | 0.281 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
nature The inheritance of the AC haplotype of rs1861972 – rs1861973, the C allele of rs1811399, and the C allele of rs1234747 may contribute to autism by affecting microRNA
[PMID 17264841] Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis.
[PMID 20174623
] Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance.
