| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1042488900 | 1.000 | 0.040 | 1 | 161802188 | synonymous variant | C/T | snv | 2 | |||
| rs10489177 | 0.925 | 0.120 | 1 | 169793666 | missense variant | T/A;G | snv | 4.1E-06; 0.19 | 4 | ||
| rs10494366 | 0.851 | 0.200 | 1 | 162115895 | intron variant | G/T | snv | 0.54 | 6 | ||
| rs1060366 | 1.000 | 0.040 | 1 | 116384040 | synonymous variant | A/G | snv | 1.3E-03 | 1.4E-03 | 2 | |
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 69 | |
| rs10911021 | 0.807 | 0.160 | 1 | 182112825 | intron variant | C/T | snv | 0.36 | 11 | ||
| rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 11 | |||
| rs1131498 | 0.732 | 0.360 | 1 | 169707345 | missense variant | A/G | snv | 0.21 | 0.22 | 13 | |
| rs11574 | 1.000 | 0.040 | 1 | 23559007 | missense variant | T/A;C | snv | 0.80 | 2 | ||
| rs11575937 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 15 | |||
| rs1205 | 0.602 | 0.680 | 1 | 159712443 | 3 prime UTR variant | C/T | snv | 0.30 | 45 | ||
| rs12144939 | 0.925 | 0.080 | 1 | 196729815 | intron variant | G/A;T | snv | 2 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs12733285 | 0.776 | 0.120 | 1 | 202952912 | intron variant | C/T | snv | 0.26 | 12 | ||
| rs1298417395 | 0.882 | 0.080 | 1 | 176206716 | missense variant | C/T | snv | 1.4E-05 | 4 | ||
| rs1342387 | 0.776 | 0.120 | 1 | 202945228 | intron variant | T/C | snv | 0.53 | 12 | ||
| rs1410996 | 0.807 | 0.240 | 1 | 196727803 | intron variant | G/A | snv | 0.46 | 5 | ||
| rs1458766475 | 0.637 | 0.680 | 1 | 169732649 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 41 | ||
| rs150924946 | 0.882 | 0.120 | 1 | 156135271 | missense variant | A/G | snv | 4.8E-04 | 1.6E-04 | 5 | |
| rs161810 | 0.925 | 0.120 | 1 | 7940737 | intron variant | T/C | snv | 0.13 | 4 | ||
| rs161827 | 1.000 | 0.040 | 1 | 7921974 | 3 prime UTR variant | T/C | snv | 0.12 | 2 | ||
| rs17106184 | 0.925 | 0.080 | 1 | 50444313 | intron variant | G/A | snv | 8.5E-02 | 3 | ||
| rs17111503 | 0.925 | 0.160 | 1 | 55037775 | upstream gene variant | A/G | snv | 0.22 | 4 | ||
| rs17568 | 0.752 | 0.320 | 1 | 1212042 | synonymous variant | C/T | snv | 0.37 | 0.31 | 12 | |
| rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 92 |