| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1000113 | 0.925 | 0.040 | 5 | 150860514 | intron variant | C/T | snv | 0.13 | 2 | ||
| rs1001007 | 0.827 | 0.120 | 3 | 46387167 | intron variant | A/G;T | snv | 5 | |||
| rs10010325 | 1.000 | 0.040 | 4 | 105185196 | intron variant | C/A;G;T | snv | 4 | |||
| rs10035653 | 1.000 | 0.040 | 5 | 442675 | non coding transcript exon variant | G/A;T | snv | 9.1E-02; 4.0E-06 | 1 | ||
| rs1004234 | 0.827 | 0.120 | 5 | 132421409 | intron variant | A/G;T | snv | 5 | |||
| rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 9 | ||
| rs10063949 | 0.882 | 0.080 | 5 | 139383837 | intron variant | T/C | snv | 0.48 | 4 | ||
| rs10094579 | 0.807 | 0.280 | 8 | 89837077 | downstream gene variant | C/A | snv | 0.18 | 6 | ||
| rs10114470 | 0.882 | 0.080 | 9 | 114785492 | 3 prime UTR variant | T/A;C | snv | 4 | |||
| rs1016883 | 1.000 | 0.040 | 2 | 198016944 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 14 | ||
| rs10185424 | 0.925 | 0.040 | 2 | 102046427 | intron variant | T/G | snv | 0.62 | 2 | ||
| rs1020856343 | 0.851 | 0.240 | 5 | 132393705 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs10226620 | 1.000 | 0.040 | 7 | 1541881 | 3 prime UTR variant | T/C | snv | 0.69 | 4 | ||
| rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
| rs10415946 | 1.000 | 0.040 | 19 | 41755151 | intron variant | A/G | snv | 0.39 | 1 | ||
| rs10416839 | 1.000 | 0.040 | 19 | 41776424 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
| 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 | |
| rs104895467 | 0.851 | 0.120 | 16 | 50716899 | missense variant | A/G | snv | 1.2E-03 | 7.5E-04 | 5 | |
| rs104895486 | 0.925 | 0.040 | 16 | 50716670 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-05 | 2 | ||
| rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
| rs1049526 | 0.925 | 0.040 | 6 | 32981027 | 3 prime UTR variant | C/T | snv | 0.93 | 3 |