| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs765508638 | 1.000 | 0.080 | 7 | 101164751 | missense variant | C/A;T | snv | 9.8E-05; 4.1E-06 | 1 | ||
| rs1209222698 | 1.000 | 0.080 | 7 | 101916177 | synonymous variant | A/G | snv | 8.0E-06 | 1 | ||
| rs2251644 | 1.000 | 0.080 | 14 | 102001510 | intron variant | A/G | snv | 0.17 | 0.21 | 1 | |
| rs941793 | 1.000 | 0.080 | 14 | 102041124 | non coding transcript exon variant | A/G | snv | 0.36 | 1 | ||
| rs115796194 | 1.000 | 0.080 | 2 | 102171877 | synonymous variant | A/G | snv | 1.1E-03 | 5.4E-03 | 1 | |
| rs745805222 | 0.790 | 0.120 | 12 | 102475722 | synonymous variant | C/T | snv | 1.2E-05 | 4.9E-05 | 7 | |
| rs748991134 | 1.000 | 0.080 | 10 | 103967838 | synonymous variant | A/G | snv | 4.0E-06 | 1 | ||
| rs536110507 | 1.000 | 0.080 | 11 | 105044573 | missense variant | C/G;T | snv | 7.0E-06 | 1 | ||
| rs752612830 | 1.000 | 0.080 | 6 | 106316116 | synonymous variant | T/C | snv | 8.0E-06 | 4.9E-05 | 1 | |
| rs1288358431 | 1.000 | 0.080 | 12 | 108592291 | synonymous variant | C/T | snv | 7.0E-06 | 1 | ||
| rs1157289563 | 0.925 | 0.120 | 9 | 108881749 | missense variant | C/T | snv | 2 | |||
| rs139166976 | 1.000 | 0.080 | 12 | 108894350 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06; 2.6E-04 | 1 | ||
| rs80356715 | 0.807 | 0.120 | 1 | 11016874 | missense variant | C/G;T | snv | 8.0E-06; 2.2E-04 | 6 | ||
| rs80356717 | 0.851 | 0.120 | 1 | 11018836 | missense variant | A/G | snv | 5 | |||
| rs267607102 | 0.851 | 0.120 | 1 | 11022196 | missense variant | A/G | snv | 5 | |||
| rs80356718 | 0.827 | 0.120 | 1 | 11022209 | missense variant | A/G | snv | 7.6E-05 | 4.9E-05 | 5 | |
| rs80356719 | 0.882 | 0.080 | 1 | 11022268 | missense variant | G/A;C | snv | 1.6E-05 | 3 | ||
| rs121908395 | 0.925 | 0.080 | 1 | 11022278 | missense variant | G/C;T | snv | 2 | |||
| rs80356721 | 0.925 | 0.080 | 1 | 11022290 | missense variant | G/A;C;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
| rs4884357 | 0.807 | 0.120 | 1 | 11022301 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs80356726 | 0.763 | 0.120 | 1 | 11022352 | splice acceptor variant | G/A | snv | 4.0E-06 | 12 | ||
| rs80356727 | 0.925 | 0.080 | 1 | 11022400 | missense variant | C/A | snv | 3 | |||
| rs80356730 | 0.807 | 0.120 | 1 | 11022418 | missense variant | A/G | snv | 8.0E-06 | 7 | ||
| rs80356732 | 0.925 | 0.080 | 1 | 11022444 | missense variant | C/A | snv | 8.0E-06 | 2 | ||
| rs80356733 | 0.790 | 0.200 | 1 | 11022451 | missense variant | G/T | snv | 7 |