Rs10836235
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10836235 |
| PheGenI | rs10836235 |
| nextbio | rs10836235 |
| hapmap | rs10836235 |
| 1000 genomes | rs10836235 |
| hgdp | rs10836235 |
| ensembl | rs10836235 |
| gopubmed | rs10836235 |
| geneview | rs10836235 |
| scholar | rs10836235 |
| rs10836235 | |
| pharmgkb | rs10836235 |
| gwascentral | rs10836235 |
| openSNP | rs10836235 |
| 23andMe | rs10836235 |
| 23andMe all | rs10836235 |
| SNP Nexus | |
| SNPshot | rs10836235 |
| SNPdbe | rs10836235 |
| MSV3d | rs10836235 |
| Gene | CAT |
| Chromosome | 11 |
| Orientation | plus |
| GMAF | 0.1534 |
| Position | 34460704 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs10836235(C;C) |
| Make rs10836235(C;T) |
| Make rs10836235(T;T) |
[PMID 19863340] Influence of the polymorphism in candidate genes on late cardiac damage in patients treated due to acute leukemia in childhood
[PMID 20416077] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.
| GET Evidence | |
|---|---|
| rs10836235 | |
| aa_change | |
| aa_change_short | |
| impact | pharmacogenetic |
| qualified_impact | Insufficiently evaluated pharmacogenetic |
| overall_frequency | 0.104839 |
| summary | |
