rs6660197
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6660197(C;C) |
| Make rs6660197(C;T) |
| Make rs6660197(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 200734413 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6660197 |
| dbSNP (classic) | rs6660197 |
| ClinGen | rs6660197 |
| ebi | rs6660197 |
| HLI | rs6660197 |
| Exac | rs6660197 |
| Gnomad | rs6660197 |
| Varsome | rs6660197 |
| LitVar | rs6660197 |
| Map | rs6660197 |
| PheGenI | rs6660197 |
| Biobank | rs6660197 |
| 1000 genomes | rs6660197 |
| hgdp | rs6660197 |
| ensembl | rs6660197 |
| geneview | rs6660197 |
| scholar | rs6660197 |
| rs6660197 | |
| pharmgkb | rs6660197 |
| gwascentral | rs6660197 |
| openSNP | rs6660197 |
| 23andMe | rs6660197 |
| SNPshot | rs6660197 |
| SNPdbe | rs6660197 |
| MSV3d | rs6660197 |
| GWAS Ctlg | rs6660197 |
| GMAF | 0.146 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22116939] Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese
