rs12744221
From SNPedia
| Orientation | minus |
| Stabilized | plus |
| Make rs12744221(C;C) |
| Make rs12744221(C;T) |
| Make rs12744221(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 145789475 |
| Gene | RNF115 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12744221 |
| dbSNP (classic) | rs12744221 |
| ClinGen | rs12744221 |
| ebi | rs12744221 |
| HLI | rs12744221 |
| Exac | rs12744221 |
| Gnomad | rs12744221 |
| Varsome | rs12744221 |
| LitVar | rs12744221 |
| Map | rs12744221 |
| PheGenI | rs12744221 |
| Biobank | rs12744221 |
| 1000 genomes | rs12744221 |
| hgdp | rs12744221 |
| ensembl | rs12744221 |
| geneview | rs12744221 |
| scholar | rs12744221 |
| rs12744221 | |
| pharmgkb | rs12744221 |
| gwascentral | rs12744221 |
| openSNP | rs12744221 |
| 23andMe | rs12744221 |
| SNPshot | rs12744221 |
| SNPdbe | rs12744221 |
| MSV3d | rs12744221 |
| GWAS Ctlg | rs12744221 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 23962720 ]
|
| Trait | Epilepsy (remission after treatment) |
| Title | A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. |
| Risk Allele | C |
| P-val | 6E-6 |
| Odds Ratio | 1.66 [NR] |
