rs533259
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs533259(C;C) |
| Make rs533259(C;T) |
| Make rs533259(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 182579884 |
| Gene | RNASEL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs533259 |
| dbSNP (classic) | rs533259 |
| ClinGen | rs533259 |
| ebi | rs533259 |
| HLI | rs533259 |
| Exac | rs533259 |
| Gnomad | rs533259 |
| Varsome | rs533259 |
| LitVar | rs533259 |
| Map | rs533259 |
| PheGenI | rs533259 |
| Biobank | rs533259 |
| 1000 genomes | rs533259 |
| hgdp | rs533259 |
| ensembl | rs533259 |
| geneview | rs533259 |
| scholar | rs533259 |
| rs533259 | |
| pharmgkb | rs533259 |
| gwascentral | rs533259 |
| openSNP | rs533259 |
| 23andMe | rs533259 |
| SNPshot | rs533259 |
| SNPdbe | rs533259 |
| MSV3d | rs533259 |
| GWAS Ctlg | rs533259 |
| GMAF | 0.107 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23412934 ]
|
| Trait | Multiple sclerosis |
| Title | A genome-wide association study of brain lesion distribution in multiple sclerosis. |
| Risk Allele | |
| P-val | 6E-9 |
| Odds Ratio | NR NR |
[PMID 18575592] Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer.
[PMID 19567509] Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
