rs10411936
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10411936(A;A) |
| Make rs10411936(A;G) |
| Make rs10411936(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 16437564 |
| Gene | EPS15L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10411936 |
| dbSNP (classic) | rs10411936 |
| ClinGen | rs10411936 |
| ebi | rs10411936 |
| HLI | rs10411936 |
| Exac | rs10411936 |
| Gnomad | rs10411936 |
| Varsome | rs10411936 |
| LitVar | rs10411936 |
| Map | rs10411936 |
| PheGenI | rs10411936 |
| Biobank | rs10411936 |
| 1000 genomes | rs10411936 |
| hgdp | rs10411936 |
| ensembl | rs10411936 |
| geneview | rs10411936 |
| scholar | rs10411936 |
| rs10411936 | |
| pharmgkb | rs10411936 |
| gwascentral | rs10411936 |
| openSNP | rs10411936 |
| 23andMe | rs10411936 |
| SNPshot | rs10411936 |
| SNPdbe | rs10411936 |
| MSV3d | rs10411936 |
| GWAS Ctlg | rs10411936 |
| GMAF | 0.3958 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22190364 |
| Trait | |
| Title | Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. |
| Risk Allele | A |
| P-val | 2E-7 |
| Odds Ratio | 1.1600 None |
| GWAS snp | |
|---|---|
| PMID | [PMID 21738480 |
| Trait | White blood cell count |
| Title | Multiple loci are associated with white blood cell phenotypes. |
| Risk Allele | A |
| P-val | 3E-12 |
| Odds Ratio | .02 [0.011-0.020] unit increase |
