rs1407131
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1407131(C;C) |
| Make rs1407131(C;T) |
| Make rs1407131(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 86912944 |
| Gene | HS2ST1, SELENOF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1407131 |
| dbSNP (classic) | rs1407131 |
| ClinGen | rs1407131 |
| ebi | rs1407131 |
| HLI | rs1407131 |
| Exac | rs1407131 |
| Gnomad | rs1407131 |
| Varsome | rs1407131 |
| LitVar | rs1407131 |
| Map | rs1407131 |
| PheGenI | rs1407131 |
| Biobank | rs1407131 |
| 1000 genomes | rs1407131 |
| hgdp | rs1407131 |
| ensembl | rs1407131 |
| geneview | rs1407131 |
| scholar | rs1407131 |
| rs1407131 | |
| pharmgkb | rs1407131 |
| gwascentral | rs1407131 |
| openSNP | rs1407131 |
| 23andMe | rs1407131 |
| SNPshot | rs1407131 |
| SNPdbe | rs1407131 |
| MSV3d | rs1407131 |
| GWAS Ctlg | rs1407131 |
| GMAF | 0.1079 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20424130
] A Large Prospective Study of SEP15 Genetic Variation, Interaction with Plasma Selenium Levels, and Prostate Cancer Risk and Survival
[PMID 19680542] Tissue effect on genetic control of transcript isoform variation.
