| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11554137 | 0.742 | 0.040 | 2 | 208248468 | synonymous variant | G/A | snv | 5.1E-02 | 6.8E-02 | 13 | |
| rs753152604 | 0.827 | 0.040 | 12 | 57751680 | missense variant | C/A | snv | 7 | |||
| rs1373481065 | 0.827 | 0.040 | 1 | 67687668 | missense variant | A/G | snv | 4.0E-06 | 6 | ||
| rs1005230 | 0.827 | 0.040 | 6 | 43768759 | upstream gene variant | T/C | snv | 0.60 | 5 | ||
| rs11860248 | 0.882 | 0.040 | 16 | 24566445 | intron variant | T/G | snv | 0.27 | 5 | ||
| rs1385943435 | 0.851 | 0.040 | 9 | 37002662 | missense variant | C/A;G;T | snv | 4.1E-06; 4.1E-06 | 5 | ||
| rs2234248 | 0.827 | 0.040 | 6 | 41163980 | upstream gene variant | A/G | snv | 2.2E-03 | 5 | ||
| rs3092993 | 0.827 | 0.040 | 11 | 108364388 | intron variant | C/A | snv | 0.11 | 5 | ||
| rs374052197 | 0.882 | 0.040 | 1 | 13610421 | missense variant | G/A;T | snv | 8.0E-06 | 5 | ||
| rs374524467 | 0.827 | 0.040 | 4 | 110632961 | missense variant | A/C | snv | 8.0E-06 | 7.0E-06 | 5 | |
| rs71305152 | 0.882 | 0.040 | 8 | 105437494 | intron variant | -/TTTTCT | delins | 0.43 | 5 | ||
| rs745934102 | 0.882 | 0.040 | 1 | 13607281 | missense variant | G/A | snv | 3.2E-05 | 1.4E-05 | 5 | |
| rs760031382 | 0.851 | 0.040 | 9 | 36966613 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
| rs865880036 | 0.827 | 0.040 | 15 | 37098156 | missense variant | A/C | snv | 1.3E-04 | 5 | ||
| rs1920116 | 0.882 | 0.040 | 3 | 169862183 | intron variant | G/A | snv | 0.25 | 4 | ||
| rs2252586 | 0.882 | 0.040 | 7 | 54911231 | intergenic variant | C/T | snv | 0.27 | 4 | ||
| rs10131 | 1.000 | 0.040 | 13 | 108207498 | 3 prime UTR variant | C/T | snv | 0.12 | 3 | ||
| rs1052555 | 0.882 | 0.040 | 19 | 45352266 | synonymous variant | G/A | snv | 0.28 | 0.26 | 3 | |
| rs11079041 | 0.882 | 0.040 | 17 | 42262061 | intron variant | T/A;C | snv | 0.36 | 3 | ||
| rs117677079 | 0.882 | 0.040 | 4 | 121673909 | intron variant | T/C | snv | 8.3E-03 | 3 | ||
| rs13332653 | 0.882 | 0.040 | 16 | 24578078 | intergenic variant | T/G | snv | 0.11 | 3 | ||
| rs1346787 | 0.882 | 0.040 | 2 | 55865477 | downstream gene variant | C/A;G;T | snv | 3 | |||
| rs1801591 | 0.882 | 0.040 | 15 | 76286421 | missense variant | G/A | snv | 7.4E-02 | 6.4E-02 | 3 | |
| rs2033214 | 0.882 | 0.040 | 16 | 24566199 | intron variant | T/G | snv | 0.14 | 3 | ||
| rs6470745 | 0.882 | 0.040 | 8 | 129629675 | intron variant | A/G | snv | 0.18 | 3 |