| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
| rs10431923 | 0.925 | 0.120 | 16 | 68805360 | intron variant | G/T | snv | 0.44 | 2 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs1047781 | 0.790 | 0.200 | 19 | 48703374 | missense variant | A/T | snv | 3.6E-02 | 1.2E-02 | 11 | |
| rs1048230 | 0.827 | 0.160 | 12 | 50992283 | synonymous variant | A/G | snv | 0.17 | 0.15 | 5 | |
| rs10484545 | 1.000 | 0.040 | 6 | 29266733 | intron variant | C/A;G | snv | 1 | |||
| rs10486483 | 1.000 | 0.040 | 7 | 26852821 | intron variant | G/A | snv | 0.21 | 2 | ||
| rs10489276 | 1.000 | 0.040 | 1 | 172893799 | intron variant | C/T | snv | 0.31 | 1 | ||
| rs104895420 | 1.000 | 0.040 | 16 | 50699883 | missense variant | T/C | snv | 1.3E-04 | 5.6E-05 | 1 | |
| rs104895422 | 1.000 | 0.040 | 16 | 50710614 | missense variant | C/T | snv | 1.0E-04 | 1.3E-04 | 1 | |
| rs104895423 | 1.000 | 0.040 | 16 | 50710654 | missense variant | T/G | snv | 5.6E-04 | 2.6E-04 | 1 | |
| rs104895424 | 1.000 | 0.040 | 16 | 50710782 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs104895425 | 1.000 | 0.040 | 16 | 50710792 | missense variant | C/G | snv | 1.9E-03 | 1.5E-03 | 1 | |
| rs104895426 | 1.000 | 0.040 | 16 | 50710813 | missense variant | C/T | snv | 4.4E-05 | 4.2E-05 | 1 | |
| rs104895427 | 1.000 | 0.040 | 16 | 50710842 | missense variant | C/A;T | snv | 5.9E-04 | 1 | ||
| rs104895428 | 1.000 | 0.040 | 16 | 50710953 | missense variant | C/G | snv | 1 | |||
| rs104895429 | 1.000 | 0.040 | 16 | 50711152 | missense variant | A/C;G | snv | 4.0E-06; 7.2E-05 | 1 | ||
| rs104895431 | 1.000 | 0.040 | 16 | 50711203 | missense variant | C/T | snv | 9.7E-04 | 1.0E-03 | 1 | |
| rs104895432 | 1.000 | 0.040 | 16 | 50711232 | missense variant | G/A | snv | 3.1E-04 | 3.3E-04 | 1 | |
| rs104895438 | 0.925 | 0.120 | 16 | 50711745 | missense variant | G/A;T | snv | 6.4E-04; 5.6E-05 | 2 | ||
| rs104895439 | 1.000 | 0.040 | 16 | 50711746 | missense variant | C/T | snv | 1.6E-05 | 1 | ||
| rs104895440 | 1.000 | 0.040 | 16 | 50712048 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs104895442 | 1.000 | 0.040 | 16 | 50712184 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs104895443 | 1.000 | 0.040 | 16 | 50712243 | missense variant | G/A | snv | 2.4E-04 | 2.0E-04 | 1 | |
| rs104895444 | 1.000 | 0.040 | 16 | 50712288 | missense variant | G/A;T | snv | 1.1E-03 | 1 |