rs2292096
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2292096(A;A) |
| Make rs2292096(A;G) |
| Make rs2292096(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 200857641 |
| Gene | CAMSAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2292096 |
| dbSNP (classic) | rs2292096 |
| ClinGen | rs2292096 |
| ebi | rs2292096 |
| HLI | rs2292096 |
| Exac | rs2292096 |
| Gnomad | rs2292096 |
| Varsome | rs2292096 |
| LitVar | rs2292096 |
| Map | rs2292096 |
| PheGenI | rs2292096 |
| Biobank | rs2292096 |
| 1000 genomes | rs2292096 |
| hgdp | rs2292096 |
| ensembl | rs2292096 |
| geneview | rs2292096 |
| scholar | rs2292096 |
| rs2292096 | |
| pharmgkb | rs2292096 |
| gwascentral | rs2292096 |
| openSNP | rs2292096 |
| 23andMe | rs2292096 |
| SNPshot | rs2292096 |
| SNPdbe | rs2292096 |
| MSV3d | rs2292096 |
| GWAS Ctlg | rs2292096 |
| GMAF | 0.1515 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22116939] |
| Trait | |
| Title | Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. |
| Risk Allele | |
| P-val | 1E-8 |
| Odds Ratio | 1.5900 None |
[PMID 24148305] The potential role of CAMSAP1L1 in symptomatic epilepsy
