rs998592
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs998592(A;A) |
| Make rs998592(A;G) |
| Make rs998592(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 11105821 |
| Gene | CLEC16A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs998592 |
| dbSNP (classic) | rs998592 |
| ClinGen | rs998592 |
| ebi | rs998592 |
| HLI | rs998592 |
| Exac | rs998592 |
| Gnomad | rs998592 |
| Varsome | rs998592 |
| LitVar | rs998592 |
| Map | rs998592 |
| PheGenI | rs998592 |
| Biobank | rs998592 |
| 1000 genomes | rs998592 |
| hgdp | rs998592 |
| ensembl | rs998592 |
| geneview | rs998592 |
| scholar | rs998592 |
| rs998592 | |
| pharmgkb | rs998592 |
| gwascentral | rs998592 |
| openSNP | rs998592 |
| 23andMe | rs998592 |
| SNPshot | rs998592 |
| SNPdbe | rs998592 |
| MSV3d | rs998592 |
| GWAS Ctlg | rs998592 |
| GMAF | 0.348 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20849399] More CLEC16A gene variants associated with multiple sclerosis
[PMID 22534877] Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance
