| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs63750416 | 0.851 | 0.120 | 17 | 46010373 | missense variant | A/C | snv | 7 | |||
| rs201106962 | 0.851 | 0.080 | 4 | 89828156 | missense variant | A/C | snv | 8.0E-05 | 7.0E-05 | 5 | |
| rs886039227 | 0.925 | 0.200 | 2 | 74378123 | missense variant | A/C | snv | 4 | |||
| rs421016 | 0.683 | 0.440 | 1 | 155235252 | missense variant | A/C;G | snv | 8.0E-06; 1.3E-03 | 30 | ||
| rs767543900 | 0.790 | 0.120 | 17 | 45971879 | missense variant | A/C;G | snv | 4.0E-06 | 10 | ||
| rs775809722 | 1.000 | 0.040 | 1 | 20633925 | missense variant | A/C;G | snv | 5.3E-06; 3.7E-05 | 2 | ||
| rs139548132 | 1.000 | 1 | 119140608 | missense variant | A/C;G;T | snv | 3.2E-03; 1.6E-05; 4.0E-06 | 2 | |||
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs63750590 | 0.790 | 0.120 | 14 | 73186860 | missense variant | A/G | snv | 10 | |||
| rs35801418 | 0.827 | 0.120 | 12 | 40321114 | missense variant | A/G | snv | 7 | |||
| rs387907571 | 0.827 | 0.080 | 3 | 132477995 | missense variant | A/G | snv | 4.2E-06 | 3.5E-05 | 6 | |
| rs121917763 | 0.925 | 0.040 | 11 | 2167896 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 5 | |
| rs63750072 | 1.000 | 0.080 | 17 | 45983493 | missense variant | A/G | snv | 4.0E-02 | 3.8E-02 | 3 | |
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs41311141 | 22 | 32484019 | synonymous variant | A/G;T | snv | 3.4E-02 | 1 | ||||
| rs137852538 | 0.925 | 0.080 | X | 78117385 | missense variant | A/T | snv | 3 | |||
| rs752078407 | 1.000 | 0.080 | 20 | 3910806 | missense variant | A/T | snv | 6.4E-05 | 3.5E-05 | 3 | |
| rs1417802320 | 1 | 7962861 | missense variant | A/T | snv | 4.0E-06 | 1 | ||||
| rs1555507479 | 0.807 | 0.160 | 16 | 56336799 | missense variant | C/A | snv | 12 | |||
| rs74315360 | 0.925 | 0.040 | 1 | 20638104 | missense variant | C/A | snv | 3 | |||
| rs55739947 | 15 | 101010802 | missense variant | C/A | snv | 9.3E-03 | 8.4E-03 | 1 | |||
| rs33939927 | 0.708 | 0.120 | 12 | 40310434 | missense variant | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 24 | ||
| rs368134308 | 0.882 | 0.040 | 6 | 162443356 | missense variant | C/A;G;T | snv | 3.2E-05; 2.6E-04 | 4 | ||
| rs267604921 | 0.925 | 0.160 | 17 | 45993953 | missense variant | C/A;G;T | snv | 6.3E-05; 2.5E-04; 5.3E-06 | 3 | ||
| rs74315414 | 0.882 | 0.200 | 20 | 4699533 | missense variant | C/A;T | snv | 4.0E-06 | 5 |