rs374039502
From SNPedia
| Orientation | plus |
| Make rs374039502(A;A) |
| Make rs374039502(A;T) |
| Make rs374039502(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 13 |
| Position | 108308037 |
| Gene | TNFSF13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs374039502 |
| dbSNP (classic) | rs374039502 |
| ClinGen | rs374039502 |
| ebi | rs374039502 |
| HLI | rs374039502 |
| Exac | rs374039502 |
| Gnomad | rs374039502 |
| Varsome | rs374039502 |
| LitVar | rs374039502 |
| Map | rs374039502 |
| PheGenI | rs374039502 |
| Biobank | rs374039502 |
| 1000 genomes | rs374039502 |
| hgdp | rs374039502 |
| ensembl | rs374039502 |
| geneview | rs374039502 |
| scholar | rs374039502 |
| rs374039502 | |
| pharmgkb | rs374039502 |
| gwascentral | rs374039502 |
| openSNP | rs374039502 |
| 23andMe | rs374039502 |
| SNPshot | rs374039502 |
| SNPdbe | rs374039502 |
| MSV3d | rs374039502 |
| GWAS Ctlg | rs374039502 |
| Max Magnitude | 0 |
[PMID 30586461
] A TNFSF13B functional variant is not involved in systemic sclerosis and giant cell arteritis susceptibility.
