rs2736157
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs2736157 |
| dbSNP (classic) | rs2736157 |
| ClinGen | rs2736157 |
| ebi | rs2736157 |
| HLI | rs2736157 |
| Exac | rs2736157 |
| Gnomad | rs2736157 |
| Varsome | rs2736157 |
| LitVar | rs2736157 |
| Map | rs2736157 |
| PheGenI | rs2736157 |
| Biobank | rs2736157 |
| 1000 genomes | rs2736157 |
| hgdp | rs2736157 |
| ensembl | rs2736157 |
| geneview | rs2736157 |
| scholar | rs2736157 |
| rs2736157 | |
| pharmgkb | rs2736157 |
| gwascentral | rs2736157 |
| openSNP | rs2736157 |
| 23andMe | rs2736157 |
| SNPshot | rs2736157 |
| SNPdbe | rs2736157 |
| MSV3d | rs2736157 |
| GWAS Ctlg | rs2736157 |
| Max Magnitude | 0 |
[PMID 32862241] Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population.
