| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs879255514 | 0.925 | 0.080 | 17 | 44372407 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs1052533574 | 1.000 | 0.080 | 17 | 44386063 | missense variant | A/G | snv | 1 | |||
| rs1344532070 | 1.000 | 0.080 | 17 | 44375894 | missense variant | A/G | snv | 8.2E-06 | 7.0E-06 | 1 | |
| rs137852907 | 1.000 | 0.080 | 17 | 44384567 | missense variant | C/T | snv | 1 | |||
| rs137852908 | 1.000 | 0.080 | 17 | 44383630 | missense variant | C/T | snv | 1 | |||
| rs137852910 | 1.000 | 0.080 | 17 | 44383640 | missense variant | C/T | snv | 8.8E-06 | 1 | ||
| rs137852911 | 1.000 | 0.080 | 17 | 44385193 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs74475415 | 1.000 | 0.080 | 17 | 44376323 | missense variant | T/G | snv | 8.0E-06 | 1 | ||
| rs75622274 | 1.000 | 0.080 | 17 | 44381058 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs761174160 | 1.000 | 0.080 | 17 | 44377022 | missense variant | G/C | snv | 4.6E-06 | 1 | ||
| rs763762304 | 1.000 | 0.080 | 17 | 44377012 | missense variant | C/G;T | snv | 4.7E-06; 5.6E-05 | 1 | ||
| rs766006685 | 1.000 | 0.080 | 17 | 44383564 | missense variant | C/T | snv | 1 | |||
| rs766503255 | 0.882 | 0.080 | 17 | 44372408 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs76811038 | 1.000 | 0.080 | 17 | 44379780 | missense variant | A/G | snv | 6.4E-05 | 5.6E-05 | 1 | |
| rs77458039 | 1.000 | 0.080 | 17 | 44375039 | missense variant | C/A | snv | 1 | |||
| rs77961246 | 1.000 | 0.080 | 17 | 44377772 | missense variant | A/G | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 1 | |
| rs780786843 | 1.000 | 0.080 | 17 | 44381038 | missense variant | C/A;G;T | snv | 4.0E-06; 3.2E-05 | 1 | ||
| rs78657866 | 1.000 | 0.080 | 17 | 44374470 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs80002943 | 1.000 | 0.080 | 17 | 44374732 | missense variant | G/A | snv | 1 | |||
| rs121918444 | 1.000 | 0.080 | 17 | 47286364 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs121918445 | 1.000 | 0.080 | 17 | 47284514 | missense variant | G/T | snv | 1 | |||
| rs121918446 | 1.000 | 0.080 | 17 | 47286363 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs121918449 | 1.000 | 0.080 | 17 | 47291027 | missense variant | G/A | snv | 1 | |||
| rs121918452 | 1.000 | 0.080 | 17 | 47284509 | missense variant | T/G | snv | 2.0E-05 | 1 | ||
| rs13306476 | 1.000 | 0.080 | 17 | 47287209 | missense variant | A/C;G | snv | 4.0E-06; 8.0E-06 | 1 |