rs11865121
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11865121(A;A) |
| Make rs11865121(A;C) |
| Make rs11865121(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 11072831 |
| Gene | CLEC16A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11865121 |
| dbSNP (classic) | rs11865121 |
| ClinGen | rs11865121 |
| ebi | rs11865121 |
| HLI | rs11865121 |
| Exac | rs11865121 |
| Gnomad | rs11865121 |
| Varsome | rs11865121 |
| LitVar | rs11865121 |
| Map | rs11865121 |
| PheGenI | rs11865121 |
| Biobank | rs11865121 |
| 1000 genomes | rs11865121 |
| hgdp | rs11865121 |
| ensembl | rs11865121 |
| geneview | rs11865121 |
| scholar | rs11865121 |
| rs11865121 | |
| pharmgkb | rs11865121 |
| gwascentral | rs11865121 |
| openSNP | rs11865121 |
| 23andMe | rs11865121 |
| SNPshot | rs11865121 |
| SNPdbe | rs11865121 |
| MSV3d | rs11865121 |
| GWAS Ctlg | rs11865121 |
| GMAF | 0.3508 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19525953 ]
|
| Trait | Multiple sclerosis |
| Title | Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci |
| Risk Allele | C |
| P-val | 2E-7 |
| Odds Ratio | 1.15 [1.04-1.25] |
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
