| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs11583978 | 0.925 | 0.040 | 1 | 34864921 | downstream gene variant | A/C;G | snv | 2 | |||
| rs1477437491 | 0.925 | 0.040 | 1 | 162367213 | missense variant | G/A | snv | 2.8E-05 | 2 | ||
| rs17162912 | 1.000 | 0.040 | 1 | 222801584 | intergenic variant | T/C | snv | 0.11 | 1 | ||
| rs28696717 | 1.000 | 0.040 | 1 | 153493087 | intergenic variant | A/G | snv | 0.18 | 1 | ||
| rs4387163 | 1.000 | 0.040 | 1 | 165026476 | intergenic variant | G/A | snv | 0.44 | 1 | ||
| rs4652867 | 1.000 | 0.040 | 1 | 34901689 | intron variant | G/A;T | snv | 1 | |||
| rs6662980 | 1.000 | 0.040 | 1 | 34894477 | intron variant | A/G;T | snv | 1 | |||
| rs7541937 | 1.000 | 0.040 | 1 | 34876381 | intron variant | T/G | snv | 0.47 | 1 | ||
| rs1000592 | 1.000 | 0.040 | 2 | 118939624 | upstream gene variant | C/A | snv | 6.4E-03 | 1 | ||
| rs2254298 | 0.701 | 0.200 | 3 | 8760542 | intron variant | G/A | snv | 0.16 | 23 | ||
| rs13316193 | 0.882 | 0.040 | 3 | 8761057 | intron variant | T/C | snv | 0.45 | 4 | ||
| rs2268493 | 0.882 | 0.040 | 3 | 8759154 | intron variant | T/C | snv | 0.25 | 3 | ||
| rs2268490 | 1.000 | 0.040 | 3 | 8755399 | intron variant | C/T | snv | 0.18 | 2 | ||
| rs237887 | 1.000 | 0.040 | 3 | 8755356 | intron variant | G/A;C | snv | 2 | |||
| rs4686301 | 1.000 | 0.040 | 3 | 8756900 | intron variant | C/T | snv | 0.27 | 2 | ||
| rs4988462 | 0.925 | 0.120 | 3 | 87264203 | intron variant | C/T | snv | 0.31 | 2 | ||
| rs6766410 | 1.000 | 0.040 | 3 | 184056974 | missense variant | C/A;T | snv | 0.45; 4.0E-06 | 2 | ||
| rs7627615 | 0.925 | 0.040 | 3 | 184100628 | missense variant | G/A;C | snv | 0.64; 4.0E-06 | 2 | ||
| rs1000952 | 1.000 | 0.040 | 3 | 184038034 | missense variant | G/A;C;T | snv | 0.66; 3.6E-05; 4.0E-06 | 1 | ||
| rs12635725 | 1.000 | 0.040 | 3 | 1895465 | intergenic variant | A/G;T | snv | 1 | |||
| rs1265692223 | 1.000 | 0.040 | 3 | 184100530 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs6443930 | 1.000 | 0.040 | 3 | 184036506 | splice donor variant | G/A;C;T | snv | 0.46; 8.0E-06 | 1 | ||
| rs7628229 | 1.000 | 0.040 | 3 | 184036872 | missense variant | C/G;T | snv | 6.4E-06; 2.7E-03 | 9.5E-03 | 1 |