rs2172802
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2172802(A;A) |
| Make rs2172802(A;G) |
| Make rs2172802(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 61587491 |
| Gene | ADGRL3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2172802 |
| dbSNP (classic) | rs2172802 |
| ClinGen | rs2172802 |
| ebi | rs2172802 |
| HLI | rs2172802 |
| Exac | rs2172802 |
| Gnomad | rs2172802 |
| Varsome | rs2172802 |
| LitVar | rs2172802 |
| Map | rs2172802 |
| PheGenI | rs2172802 |
| Biobank | rs2172802 |
| 1000 genomes | rs2172802 |
| hgdp | rs2172802 |
| ensembl | rs2172802 |
| geneview | rs2172802 |
| scholar | rs2172802 |
| rs2172802 | |
| pharmgkb | rs2172802 |
| gwascentral | rs2172802 |
| openSNP | rs2172802 |
| 23andMe | rs2172802 |
| SNPshot | rs2172802 |
| SNPdbe | rs2172802 |
| MSV3d | rs2172802 |
| GWAS Ctlg | rs2172802 |
| GMAF | 0.4421 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20522523 ]
|
| Trait | Partial epilepsies |
| Title | Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | None None |
