rs2041670
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2041670(C;C) |
| Make rs2041670(C;T) |
| Make rs2041670(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 11080795 |
| Gene | CLEC16A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2041670 |
| dbSNP (classic) | rs2041670 |
| ClinGen | rs2041670 |
| ebi | rs2041670 |
| HLI | rs2041670 |
| Exac | rs2041670 |
| Gnomad | rs2041670 |
| Varsome | rs2041670 |
| LitVar | rs2041670 |
| Map | rs2041670 |
| PheGenI | rs2041670 |
| Biobank | rs2041670 |
| 1000 genomes | rs2041670 |
| hgdp | rs2041670 |
| ensembl | rs2041670 |
| geneview | rs2041670 |
| scholar | rs2041670 |
| rs2041670 | |
| pharmgkb | rs2041670 |
| gwascentral | rs2041670 |
| openSNP | rs2041670 |
| 23andMe | rs2041670 |
| SNPshot | rs2041670 |
| SNPdbe | rs2041670 |
| MSV3d | rs2041670 |
| GWAS Ctlg | rs2041670 |
| GMAF | 0.3388 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20849399] More CLEC16A gene variants associated with multiple sclerosis
[PMID 18840781
] Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
