rs8049439
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8049439(C;C) |
| Make rs8049439(C;T) |
| Make rs8049439(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 28826194 |
| Gene | ATXN2L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8049439 |
| dbSNP (classic) | rs8049439 |
| ClinGen | rs8049439 |
| ebi | rs8049439 |
| HLI | rs8049439 |
| Exac | rs8049439 |
| Gnomad | rs8049439 |
| Varsome | rs8049439 |
| LitVar | rs8049439 |
| Map | rs8049439 |
| PheGenI | rs8049439 |
| Biobank | rs8049439 |
| 1000 genomes | rs8049439 |
| hgdp | rs8049439 |
| ensembl | rs8049439 |
| geneview | rs8049439 |
| scholar | rs8049439 |
| rs8049439 | |
| pharmgkb | rs8049439 |
| gwascentral | rs8049439 |
| openSNP | rs8049439 |
| 23andMe | rs8049439 |
| SNPshot | rs8049439 |
| SNPdbe | rs8049439 |
| MSV3d | rs8049439 |
| GWAS Ctlg | rs8049439 |
| GMAF | 0.3581 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19915574 ]
|
| Trait | Inflammatory bowel disease (early onset) |
| Title | Common variants at five new loci associated with early-onset inflammatory bowel disease |
| Risk Allele | G |
| P-val | 2E-9 |
| Odds Ratio | 1.14 [1.00-1.30] |
[PMID 20473688] Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children
[PMID 19478790] The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI.
| GWAS snp | |
|---|---|
| PMID | [PMID 23722424]
|
| Trait | Educational attainment |
| Title | GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. |
| Risk Allele | T |
| P-val | 1E-7 |
| Odds Ratio | .09 [NR] unit increase |
