| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13293512 | 0.763 | 0.360 | 9 | 94167461 | intron variant | T/C | snv | 0.24 | 11 | ||
| rs1746048 | 0.776 | 0.120 | 10 | 44280376 | downstream gene variant | C/T | snv | 0.25 | 8 | ||
| rs1626340 | 0.827 | 0.120 | 9 | 99161090 | intergenic variant | G/A;T | snv | 5 | |||
| rs8087799 | 0.882 | 0.080 | 18 | 22605468 | regulatory region variant | G/A | snv | 0.43 | 3 | ||
| rs10958409 | 1.000 | 0.080 | 8 | 54414531 | intergenic variant | G/A | snv | 0.18 | 2 | ||
| rs10230207 | 1.000 | 0.080 | 7 | 19571684 | intron variant | G/C;T | snv | 1 | |||
| rs1072737 | 1.000 | 0.080 | 8 | 54501764 | intergenic variant | T/G | snv | 0.36 | 1 | ||
| rs10819634 | 1.000 | 0.080 | 9 | 99097794 | intergenic variant | C/T | snv | 0.22 | 1 | ||
| rs10943471 | 1.000 | 0.080 | 6 | 77560245 | intergenic variant | A/G | snv | 0.22 | 1 | ||
| rs11661542 | 1.000 | 0.080 | 18 | 22643732 | upstream gene variant | C/A | snv | 0.38 | 1 | ||
| rs11662668 | 1.000 | 0.080 | 18 | 22599418 | intergenic variant | G/A;T | snv | 0.38 | 1 | ||
| rs12058987 | 1.000 | 0.080 | 1 | 217247673 | intergenic variant | C/A;T | snv | 1 | |||
| rs12350582 | 1.000 | 0.080 | 9 | 16135144 | intergenic variant | A/G | snv | 0.26 | 1 | ||
| rs1504749 | 1.000 | 0.080 | 8 | 54398151 | downstream gene variant | A/C | snv | 0.30 | 1 | ||
| rs17688188 | 1.000 | 0.080 | 4 | 176549908 | regulatory region variant | G/A | snv | 0.21 | 1 | ||
| rs1930095 | 1.000 | 0.080 | 9 | 108592638 | intergenic variant | T/C | snv | 0.50 | 1 | ||
| rs2374513 | 1.000 | 0.080 | 12 | 105613522 | intergenic variant | C/T | snv | 0.12 | 1 | ||
| rs3900446 | 1.000 | 0.080 | 5 | 122090980 | intergenic variant | A/G;T | snv | 1 | |||
| rs3932338 | 1.000 | 0.080 | 5 | 23742867 | regulatory region variant | G/A | snv | 0.48 | 1 | ||
| rs4667622 | 1.000 | 0.080 | 2 | 170147675 | regulatory region variant | G/A | snv | 0.50 | 1 | ||
| rs4800418 | 1.000 | 0.080 | 18 | 22566777 | intergenic variant | A/C | snv | 0.28 | 1 | ||
| rs763497 | 1.000 | 0.080 | 5 | 122091535 | regulatory region variant | A/G | snv | 0.22 | 1 | ||
| rs767603 | 1.000 | 0.080 | 14 | 60631965 | intergenic variant | T/A;C | snv | 1 | |||
| rs2230806 | 0.689 | 0.280 | 9 | 104858586 | missense variant | C/T | snv | 0.32 | 0.39 | 24 | |
| rs61748537 | 0.882 | 0.160 | 1 | 94098906 | missense variant | C/G;T | snv | 4.0E-05; 8.0E-06 | 3 |