rs1088967
From SNPedia
| Merged into | rs204340 |
| Orientation | minus |
| Stabilized | minus |
| Make rs1088967(A;A) |
| Make rs1088967(A;G) |
| Make rs1088967(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | X |
| Position | 127010099 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1088967 |
| dbSNP (classic) | rs1088967 |
| ClinGen | rs1088967 |
| ebi | rs1088967 |
| HLI | rs1088967 |
| Exac | rs1088967 |
| Gnomad | rs1088967 |
| Varsome | rs1088967 |
| LitVar | rs1088967 |
| Map | rs1088967 |
| PheGenI | rs1088967 |
| Biobank | rs1088967 |
| 1000 genomes | rs1088967 |
| hgdp | rs1088967 |
| ensembl | rs1088967 |
| geneview | rs1088967 |
| scholar | rs1088967 |
| rs1088967 | |
| pharmgkb | rs1088967 |
| gwascentral | rs1088967 |
| openSNP | rs1088967 |
| 23andMe | rs1088967 |
| SNPshot | rs1088967 |
| SNPdbe | rs1088967 |
| MSV3d | rs1088967 |
| GWAS Ctlg | rs1088967 |
| Status | Merged into rs204340 |
| Max Magnitude | 0 |
[PMID 25680555] Interleukin-17FT7488 allele is associated with a decreased risk of colorectal cancer and tumor progression
