| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1294404368 | 1.000 | 0.080 | 7 | 98981947 | missense variant | C/T | snv | 4.4E-06 | 1.4E-05 | 1 | |
| rs528967912 | 1.000 | 0.080 | 7 | 98964724 | missense variant | C/T | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs373632999 | 1.000 | 0.080 | 7 | 98949733 | missense variant | G/A | snv | 1.2E-05 | 4.2E-05 | 1 | |
| rs952665081 | 1.000 | 0.080 | 20 | 9580201 | missense variant | A/G | snv | 1 | |||
| rs140213020 | 1.000 | 0.080 | 9 | 91724870 | missense variant | C/A;T | snv | 8.2E-06; 2.0E-05 | 1 | ||
| rs1262765773 | 1.000 | 0.080 | 12 | 64485493 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs368370244 | 1.000 | 0.080 | 7 | 56087718 | missense variant | C/T | snv | 3.6E-05 | 5.6E-05 | 1 | |
| rs145602440 | 1.000 | 0.080 | 4 | 54733118 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs751005114 | 1.000 | 0.080 | 4 | 54731395 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs1407808379 | 1.000 | 0.080 | 3 | 49862154 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs781401034 | 1.000 | 0.080 | 8 | 47898527 | missense variant | C/T | snv | 1 | |||
| rs780763668 | 1.000 | 0.080 | 19 | 45280710 | missense variant | C/A;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs555460132 | 1.000 | 0.080 | 7 | 44228798 | missense variant | G/A | snv | 1.9E-04 | 2.0E-04 | 1 | |
| rs149403911 | 1.000 | 0.080 | 10 | 43102492 | missense variant | G/A;T | snv | 2.0E-05 | 1 | ||
| rs778726488 | 1.000 | 0.080 | 19 | 3778199 | missense variant | C/G;T | snv | 1.7E-05 | 1 | ||
| rs373605259 | 1.000 | 0.080 | 3 | 36737396 | missense variant | C/T | snv | 5.2E-05 | 2.1E-05 | 1 | |
| rs755089893 | 1.000 | 0.080 | 1 | 36355378 | missense variant | A/G | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs539738963 | 1.000 | 0.080 | 1 | 36348807 | missense variant | C/T | snv | 2.2E-05 | 1.4E-05 | 1 | |
| rs759012409 | 1.000 | 0.080 | 6 | 3083284 | missense variant | C/T | snv | 4.1E-06 | 7.0E-06 | 1 | |
| rs758268804 | 1.000 | 0.080 | 6 | 3077855 | missense variant | G/A | snv | 3.2E-05 | 1.0E-04 | 1 | |
| rs774996232 | 1.000 | 0.080 | 6 | 3077805 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs137853007 | 0.790 | 0.240 | 22 | 28725254 | missense variant | G/A;T | snv | 5.2E-05 | 2 | ||
| rs764534677 | 1.000 | 0.080 | 16 | 24035448 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
| rs147978363 | 1.000 | 0.080 | 16 | 22257356 | missense variant | C/T | snv | 6.7E-04 | 5.6E-04 | 1 | |
| rs376894109 | 1.000 | 0.080 | 1 | 2175293 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 |