rs2899663
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2899663(A;A) |
| Make rs2899663(A;G) |
| Make rs2899663(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 15 |
| Position | 60902035 |
| Gene | RORA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2899663 |
| dbSNP (classic) | rs2899663 |
| ClinGen | rs2899663 |
| ebi | rs2899663 |
| HLI | rs2899663 |
| Exac | rs2899663 |
| Gnomad | rs2899663 |
| Varsome | rs2899663 |
| LitVar | rs2899663 |
| Map | rs2899663 |
| PheGenI | rs2899663 |
| Biobank | rs2899663 |
| 1000 genomes | rs2899663 |
| hgdp | rs2899663 |
| ensembl | rs2899663 |
| geneview | rs2899663 |
| scholar | rs2899663 |
| rs2899663 | |
| pharmgkb | rs2899663 |
| gwascentral | rs2899663 |
| openSNP | rs2899663 |
| 23andMe | rs2899663 |
| SNPshot | rs2899663 |
| SNPdbe | rs2899663 |
| MSV3d | rs2899663 |
| GWAS Ctlg | rs2899663 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26515929
] Circadian clock-related genetic risk scores and risk of placental abruption
[PMID 27186326] Placental genetic variations in circadian clock-related genes increase the risk of placental abruption.
