rs151632
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs151632(C;C) |
| Make rs151632(C;T) |
| Make rs151632(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 3 |
| Position | 38302467 |
| Gene | SLC22A14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs151632 |
| dbSNP (classic) | rs151632 |
| ClinGen | rs151632 |
| ebi | rs151632 |
| HLI | rs151632 |
| Exac | rs151632 |
| Gnomad | rs151632 |
| Varsome | rs151632 |
| LitVar | rs151632 |
| Map | rs151632 |
| PheGenI | rs151632 |
| Biobank | rs151632 |
| 1000 genomes | rs151632 |
| hgdp | rs151632 |
| ensembl | rs151632 |
| geneview | rs151632 |
| scholar | rs151632 |
| rs151632 | |
| pharmgkb | rs151632 |
| gwascentral | rs151632 |
| openSNP | rs151632 |
| 23andMe | rs151632 |
| SNPshot | rs151632 |
| SNPdbe | rs151632 |
| MSV3d | rs151632 |
| GWAS Ctlg | rs151632 |
| Merged from | Rs1099946 |
| GMAF | 0.05601 |
| Max Magnitude | 0 |
[PMID 23528102] Association between granzyme B and perforin I polymorphisms and allograft outcomes in Hispanic kidney transplant recipients.
