| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111033563 | 0.776 | 0.240 | 6 | 26092916 | missense variant | A/C | snv | 4.0E-06 | 8 | ||
| rs80338886 | 0.882 | 0.080 | 7 | 100628228 | missense variant | A/C | snv | 3 | |||
| rs28934595 | 0.925 | 0.160 | 6 | 26091354 | missense variant | A/C | snv | 2 | |||
| rs2280673 | 0.882 | 0.160 | 3 | 133839310 | intron variant | A/C;T | snv | 3 | |||
| rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
| rs492602 | 0.925 | 0.120 | 19 | 48703160 | synonymous variant | A/G | snv | 0.38 | 0.45 | 7 | |
| rs1167115018 | 0.827 | 0.160 | 6 | 26092760 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 5 | |
| rs537002912 | 0.925 | 0.080 | 6 | 26093145 | missense variant | A/G | snv | 8.0E-06 | 2 | ||
| rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 38 | ||
| rs11558492 | 0.827 | 0.200 | 1 | 231272345 | missense variant | A/G;T | snv | 0.16 | 5 | ||
| rs1830084 | 0.882 | 0.160 | 3 | 133789620 | 3 prime UTR variant | A/G;T | snv | 4 | |||
| rs1800730 | 0.649 | 0.480 | 6 | 26090957 | missense variant | A/T | snv | 1.0E-02 | 1.0E-02 | 32 | |
| rs1561939338 | 1.000 | 0.080 | 6 | 26090839 | splice acceptor variant | AGGT/TGGAGTC | delins | 1 | |||
| rs11568350 | 0.790 | 0.240 | 2 | 189565370 | missense variant | C/A | snv | 3.8E-03 | 1.6E-02 | 9 | |
| rs35201683 | 0.732 | 0.360 | 6 | 26094205 | stop gained | C/A;T | snv | 1.4E-03 | 12 | ||
| rs763369315 | 1.000 | 0.080 | 19 | 35285003 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
| rs1424266770 | 0.790 | 0.200 | 4 | 184632307 | missense variant | C/G | snv | 8.0E-06 | 10 | ||
| rs748882267 | 0.925 | 0.080 | 6 | 26093156 | missense variant | C/G | snv | 4.0E-06 | 2 | ||
| rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
| rs780246573 | 0.732 | 0.360 | 6 | 26092860 | stop gained | C/G;T | snv | 4.0E-06; 8.0E-06 | 12 | ||
| rs781516027 | 0.882 | 0.080 | 6 | 26092744 | missense variant | C/G;T | snv | 8.0E-06; 3.6E-05 | 3 | ||
| rs1161457931 | 0.763 | 0.200 | 22 | 37084836 | missense variant | C/T | snv | 6.4E-06 | 9 | ||
| rs3817672 | 0.882 | 0.240 | 3 | 196073940 | missense variant | C/T | snv | 0.45 | 0.43 | 4 | |
| rs80338891 | 0.851 | 0.080 | 7 | 100620889 | missense variant | C/T | snv | 4.8E-05 | 5.6E-05 | 4 | |
| rs41303501 | 0.882 | 0.080 | 7 | 100629279 | missense variant | C/T | snv | 1.9E-03 | 2.1E-03 | 3 |