rs10406069
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10406069(A;A) |
| Make rs10406069(A;G) |
| Make rs10406069(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 35345627 |
| Gene | CD22, MIR5196 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10406069 |
| dbSNP (classic) | rs10406069 |
| ClinGen | rs10406069 |
| ebi | rs10406069 |
| HLI | rs10406069 |
| Exac | rs10406069 |
| Gnomad | rs10406069 |
| Varsome | rs10406069 |
| LitVar | rs10406069 |
| Map | rs10406069 |
| PheGenI | rs10406069 |
| Biobank | rs10406069 |
| 1000 genomes | rs10406069 |
| hgdp | rs10406069 |
| ensembl | rs10406069 |
| geneview | rs10406069 |
| scholar | rs10406069 |
| rs10406069 | |
| pharmgkb | rs10406069 |
| gwascentral | rs10406069 |
| openSNP | rs10406069 |
| 23andMe | rs10406069 |
| SNPshot | rs10406069 |
| SNPdbe | rs10406069 |
| MSV3d | rs10406069 |
| GWAS Ctlg | rs10406069 |
| GMAF | 0.1442 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 21961844] Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis
[PMID 21247474
] Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19.
[PMID 33245684] Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia.
