rs10181042
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10181042(C;C) |
| Make rs10181042(C;T) |
| Make rs10181042(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 60997124 |
| Gene | PUS10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10181042 |
| dbSNP (classic) | rs10181042 |
| ClinGen | rs10181042 |
| ebi | rs10181042 |
| HLI | rs10181042 |
| Exac | rs10181042 |
| Gnomad | rs10181042 |
| Varsome | rs10181042 |
| LitVar | rs10181042 |
| Map | rs10181042 |
| PheGenI | rs10181042 |
| Biobank | rs10181042 |
| 1000 genomes | rs10181042 |
| hgdp | rs10181042 |
| ensembl | rs10181042 |
| geneview | rs10181042 |
| scholar | rs10181042 |
| rs10181042 | |
| pharmgkb | rs10181042 |
| gwascentral | rs10181042 |
| openSNP | rs10181042 |
| 23andMe | rs10181042 |
| SNPshot | rs10181042 |
| SNPdbe | rs10181042 |
| MSV3d | rs10181042 |
| GWAS Ctlg | rs10181042 |
| GMAF | 0.3333 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463 |
| Trait | |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci |
| Risk Allele | T |
| P-val | 7E-9 |
| Odds Ratio | 1.1400 [1.09-1.19] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- 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
