| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1211533350 | 0.827 | 0.120 | 4 | 1805638 | synonymous variant | C/A | snv | 4.0E-06 | 7.0E-06 | 5 | |
| rs387906623 | 0.882 | 0.120 | 15 | 48460258 | missense variant | C/T | snv | 4 | |||
| rs111033552 | 0.925 | 0.120 | 6 | 116120105 | missense variant | A/G | snv | 2 | |||
| rs1314542724 | 0.925 | 0.120 | 9 | 35805595 | missense variant | C/T | snv | 2 | |||
| rs387906918 | 0.925 | 0.120 | 16 | 88804027 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
| rs756254503 | 0.925 | 0.120 | 5 | 151669740 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
| rs75790268 | 0.925 | 0.120 | 4 | 1804377 | missense variant | G/T | snv | 2 | |||
| rs770627276 | 1.000 | 0.120 | 2 | 39120412 | missense variant | T/C | snv | 2 | |||
| rs80053154 | 0.925 | 0.120 | 4 | 1805636 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs114025919 | 1.000 | 0.120 | 5 | 42688992 | missense variant | G/T | snv | 3.0E-04 | 1.1E-03 | 1 | |
| rs1179060441 | 1.000 | 0.120 | 5 | 42694934 | missense variant | C/T | snv | 8.1E-06 | 1 | ||
| rs141842220 | 1.000 | 0.120 | 20 | 5119600 | missense variant | C/T | snv | 1 | |||
| rs1448843898 | 1.000 | 0.120 | 4 | 1805608 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs145730800 | 1.000 | 0.120 | 16 | 89283963 | missense variant | G/A | snv | 5.2E-05 | 1.4E-04 | 1 | |
| rs151241066 | 1.000 | 0.120 | 1 | 220143003 | missense variant | G/A | snv | 2.0E-05 | 3.5E-05 | 1 | |
| rs201151136 | 1.000 | 0.120 | 8 | 19458486 | missense variant | T/C | snv | 1.4E-04 | 1.2E-04 | 1 | |
| rs33958176 | 1.000 | 0.120 | 15 | 98911384 | missense variant | G/A | snv | 1.6E-03 | 1.7E-03 | 1 | |
| rs540473875 | 1.000 | 0.120 | 5 | 42718502 | missense variant | A/G | snv | 4.1E-04 | 4.2E-05 | 1 | |
| rs577421663 | 1.000 | 0.120 | 5 | 42695051 | missense variant | G/A | snv | 2.0E-05 | 9.8E-05 | 1 | |
| rs577492 | 1.000 | 0.120 | 1 | 156130948 | intron variant | T/C | snv | 0.22 | 1 | ||
| rs75028043 | 1.000 | 0.120 | 5 | 42688959 | missense variant | C/T | snv | 2.1E-04 | 2.1E-05 | 1 | |
| rs751213196 | 1.000 | 0.120 | 4 | 1805602 | missense variant | G/A;T | snv | 1.2E-05; 4.0E-06 | 1 | ||
| rs754740382 | 1.000 | 0.120 | 6 | 49459175 | missense variant | T/C;G | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs780108348 | 1.000 | 0.120 | 2 | 15402229 | stop gained | G/A | snv | 1.2E-05 | 4.2E-05 | 1 | |
| rs1566902569 | 0.882 | 0.160 | 15 | 48460299 | missense variant | C/A | snv | 9 |