rs4939364
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4939364(A;A) |
| Make rs4939364(A;G) |
| Make rs4939364(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 60464852 |
| Gene | MS4A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4939364 |
| dbSNP (classic) | rs4939364 |
| ClinGen | rs4939364 |
| ebi | rs4939364 |
| HLI | rs4939364 |
| Exac | rs4939364 |
| Gnomad | rs4939364 |
| Varsome | rs4939364 |
| LitVar | rs4939364 |
| Map | rs4939364 |
| PheGenI | rs4939364 |
| Biobank | rs4939364 |
| 1000 genomes | rs4939364 |
| hgdp | rs4939364 |
| ensembl | rs4939364 |
| geneview | rs4939364 |
| scholar | rs4939364 |
| rs4939364 | |
| pharmgkb | rs4939364 |
| gwascentral | rs4939364 |
| openSNP | rs4939364 |
| 23andMe | rs4939364 |
| SNPshot | rs4939364 |
| SNPdbe | rs4939364 |
| MSV3d | rs4939364 |
| GWAS Ctlg | rs4939364 |
| GMAF | 0.3747 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21961844] Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis
