| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913083 | 1.000 | 0.040 | 10 | 89008907 | missense variant | A/G | snv | 2 | |||
| rs121913084 | 1.000 | 0.040 | 10 | 89010779 | missense variant | T/C | snv | 2 | |||
| rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
| rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 2 | ||
| rs6503659 | 1.000 | 0.040 | 17 | 41741012 | intergenic variant | A/C;G;T | snv | 2 | |||
| rs1064793400 | 1.000 | 0.040 | 3 | 37048550 | missense variant | G/A | snv | 1 | |||
| rs1064793981 | 1.000 | 0.040 | 2 | 47475030 | missense variant | G/A | snv | 1 | |||
| rs121913230 | 1.000 | 0.040 | 7 | 55181437 | missense variant | G/A | snv | 1 | |||
| rs121913431 | 1.000 | 0.040 | 7 | 55181438 | missense variant | G/A | snv | 1 | |||
| rs1295445617 | 1.000 | 0.040 | 2 | 47403398 | synonymous variant | G/A;C;T | snv | 4.5E-06; 4.5E-06 | 1 | ||
| rs149906873 | 1.000 | 0.040 | 15 | 28088564 | intron variant | G/A | snv | 1 | |||
| rs201125580 | 1.000 | 0.040 | 9 | 95467191 | missense variant | C/A;T | snv | 4.0E-06; 3.8E-04 | 1 | ||
| rs45549733 | 1.000 | 0.040 | 11 | 67586503 | missense variant | C/G;T | snv | 7.6E-05 | 1 | ||
| rs62246017 | 1.000 | 0.040 | 3 | 71433933 | intron variant | G/A;C | snv | 1 | |||
| rs7250795 | 1.000 | 0.040 | 19 | 11978928 | missense variant | C/G;T | snv | 4.0E-06; 1.7E-02 | 1 | ||
| rs764496629 | 1.000 | 0.040 | 3 | 12590859 | missense variant | C/T | snv | 1 | |||
| rs771590775 | 1.000 | 0.040 | 5 | 1294350 | missense variant | C/A;G | snv | 1 | |||
| rs773132865 | 1.000 | 0.040 | 16 | 30783312 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs774121564 | 1.000 | 0.040 | 2 | 275197 | missense variant | C/G | snv | 4.1E-06 | 1 | ||
| rs779417284 | 1.000 | 0.040 | 9 | 95449149 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
| rs879576 | 1.000 | 0.040 | 22 | 17108356 | missense variant | G/A;C | snv | 0.11 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs577715207 | 0.827 | 0.160 | 3 | 189886413 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 8 | |
| rs1256046734 | 0.763 | 0.280 | 1 | 65621409 | missense variant | A/G | snv | 7.0E-06 | 12 | ||
| rs756340448 | 0.790 | 0.240 | 19 | 45369135 | synonymous variant | G/A | snv | 4.0E-06 | 7.0E-06 | 8 |