rs11932595
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11932595(A;A) |
| Make rs11932595(A;G) |
| Make rs11932595(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 55457430 |
| Gene | CLOCK |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11932595 |
| dbSNP (classic) | rs11932595 |
| ClinGen | rs11932595 |
| ebi | rs11932595 |
| HLI | rs11932595 |
| Exac | rs11932595 |
| Gnomad | rs11932595 |
| Varsome | rs11932595 |
| LitVar | rs11932595 |
| Map | rs11932595 |
| PheGenI | rs11932595 |
| Biobank | rs11932595 |
| 1000 genomes | rs11932595 |
| hgdp | rs11932595 |
| ensembl | rs11932595 |
| geneview | rs11932595 |
| scholar | rs11932595 |
| rs11932595 | |
| pharmgkb | rs11932595 |
| gwascentral | rs11932595 |
| openSNP | rs11932595 |
| 23andMe | rs11932595 |
| SNPshot | rs11932595 |
| SNPdbe | rs11932595 |
| MSV3d | rs11932595 |
| GWAS Ctlg | rs11932595 |
| GMAF | 0.3264 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20149345] CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations
[PMID 17696255
] Common genetic variations in CLOCK transcription factor are associated with nonalcoholic fatty liver disease.
[PMID 18541547] Genetic variants of Clock transcription factor are associated with individual susceptibility to obesity.
[PMID 24332565
] Sleep and sadness: exploring the relation among sleep, cognitive control, and depressive symptoms in young adults
[PMID 24919398] Breast cancer risk, night work and circadian clock gene polymorphisms
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 4
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
