rs7999348
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7999348(A;A) |
| Make rs7999348(A;G) |
| Make rs7999348(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 99280668 |
| Gene | UBAC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7999348 |
| dbSNP (classic) | rs7999348 |
| ClinGen | rs7999348 |
| ebi | rs7999348 |
| HLI | rs7999348 |
| Exac | rs7999348 |
| Gnomad | rs7999348 |
| Varsome | rs7999348 |
| LitVar | rs7999348 |
| Map | rs7999348 |
| PheGenI | rs7999348 |
| Biobank | rs7999348 |
| 1000 genomes | rs7999348 |
| hgdp | rs7999348 |
| ensembl | rs7999348 |
| geneview | rs7999348 |
| scholar | rs7999348 |
| rs7999348 | |
| pharmgkb | rs7999348 |
| gwascentral | rs7999348 |
| openSNP | rs7999348 |
| 23andMe | rs7999348 |
| SNPshot | rs7999348 |
| SNPdbe | rs7999348 |
| MSV3d | rs7999348 |
| GWAS Ctlg | rs7999348 |
| GMAF | 0.4798 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21918955
] A putative functional variant within the ubiquitin-associated domain-containing protein 2 gene (UBAC2) is associated with increased risk of Behçet's disease
