Other complications of cardiac and vascular prosthetic devices, implants and grafts
T82.8
Case/Control GWAS ⓘ
Statistics
| Case | Control |
|---|---|
| 1441 | 458764 |
Top SNP Information
| Location | SNP | Gene | Ref>Alt | Alt in Case | Alt in Control | Chi-square | P-value | Odds Ratio |
|---|---|---|---|---|---|---|---|---|
| chr4:162737045 | rs114495584 | FSTL5 | G>A | 81 | 13912 | 30.39 | 3.528e-08 | 1.846 |
| chr16:845819 | rs2294446 | CHTF18 | A>G | 146 | 29669 | 28.35 | 1.01e-07 | 1.567 |
| chr9:22088260 | rs10757272 | - | C>T | 1644 | 470117 | 26.51 | 2.627e-07 | 1.204 |
| chr9:22098574 | rs4977574 | - | A>G | 1643 | 468791 | 25.52 | 4.385e-07 | 1.199 |
| chr9:22096055 | rs10757274 | - | A>G | 1644 | 470921 | 25.28 | 4.953e-07 | 1.198 |
| chr9:22115959 | rs2383207 | - | G>A | 1335 | 460715 | 23.94 | 9.955e-07 | 0.8374 |
| chr9:22125347 | rs1333048 | - | A>C | 1673 | 481997 | 23.21 | 1.453e-06 | 1.19 |
| chr6:160625231 | rs4709408 | SLC22A2 | C>T | 210 | 47645 | 22.84 | 1.76e-06 | 1.406 |
| chr9:22083404 | rs1333040 | - | T>C | 1151 | 400474 | 22.7 | 1.893e-06 | 0.8378 |
| chr11:796540 | rs117220114 | SLC25A22 | G>A | 177 | 39206 | 22.19 | 2.475e-06 | 1.438 |
| chr2:37593243 | rs11903018 | QPCT | T>C | 837 | 226873 | 22.04 | 2.666e-06 | 1.209 |
| chr10:113533756 | rs79991647 | - | C>T | 78 | 14478 | 22.04 | 2.675e-06 | 1.705 |
| chr11:69557652 | rs55824937 | - | G>A | 82 | 15479 | 21.55 | 3.448e-06 | 1.674 |
| chr5:33951693 | rs16891982 | SLC45A2 | G>C | 278 | 66783 | 20.74 | 5.27e-06 | 1.331 |
| chr16:814058 | rs9927389 | MSLN | C>T | 109 | 22228 | 20.6 | 5.651e-06 | 1.553 |
| chr9:22124477 | rs10757278 | - | A>G | 1611 | 464502 | 20.36 | 6.408e-06 | 1.176 |
| chr5:33955673 | rs35391 | SLC45A2 | C>T | 181 | 40801 | 20.32 | 6.555e-06 | 1.411 |
| chr9:22081850 | rs6475606 | - | C>T | 1665 | 482617 | 20.12 | 7.279e-06 | 1.175 |
| chr9:22125503 | rs1333049 | - | G>C | 1613 | 464838 | 20.03 | 7.623e-06 | 1.174 |
| chr5:33958959 | rs28777 | SLC45A2 | A>C | 240 | 56755 | 19.94 | 7.993e-06 | 1.349 |
Associated Phenotypes ⓘ
| ID | Name | Top Correlation |
|---|---|---|
| HP: 0000118 | Phenotypic abnormality | 1/20 |
| HP: 0000765 | Abnormality of the thorax | 9/20 |
| HP: 0100749 | Chest pain | 11/20 |