rs485499
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs485499(C;C) |
| Make rs485499(C;T) |
| Make rs485499(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 160028076 |
| Gene | IL12A-AS1, LINC01100 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs485499 |
| dbSNP (classic) | rs485499 |
| ClinGen | rs485499 |
| ebi | rs485499 |
| HLI | rs485499 |
| Exac | rs485499 |
| Gnomad | rs485499 |
| Varsome | rs485499 |
| LitVar | rs485499 |
| Map | rs485499 |
| PheGenI | rs485499 |
| Biobank | rs485499 |
| 1000 genomes | rs485499 |
| hgdp | rs485499 |
| ensembl | rs485499 |
| geneview | rs485499 |
| scholar | rs485499 |
| rs485499 | |
| pharmgkb | rs485499 |
| gwascentral | rs485499 |
| openSNP | rs485499 |
| 23andMe | rs485499 |
| SNPshot | rs485499 |
| SNPdbe | rs485499 |
| MSV3d | rs485499 |
| GWAS Ctlg | rs485499 |
| GMAF | 0.2241 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21399635 ]
|
| Trait | |
| Title | Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis |
| Risk Allele | T |
| P-val | 2E-16 |
| Odds Ratio | 1.3800 [1.28-1.50] |
