| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs936551 | 1.000 | 0.200 | 4 | 827702 | upstream gene variant | A/G | snv | 0.52 | 1 | ||
| rs13154629 | 1.000 | 0.200 | 5 | 96786754 | non coding transcript exon variant | C/T | snv | 0.16 | 1 | ||
| rs1065407 | 1.000 | 0.200 | 5 | 96776379 | 3 prime UTR variant | T/A;G | snv | 3.3E-05; 0.26 | 1 | ||
| rs943899383 | 1.000 | 0.200 | 1 | 169586343 | frameshift variant | C/- | delins | 1 | |||
| rs9577873 | 1.000 | 0.200 | 13 | 113825282 | intron variant | G/A;T | snv | 1 | |||
| rs9260997 | 1.000 | 0.200 | 6 | 29995539 | upstream gene variant | T/C | snv | 0.90 | 1 | ||
| rs4394274 | 1.000 | 0.200 | 6 | 31350387 | intron variant | C/A | snv | 0.40 | 1 | ||
| rs6940 | 1.000 | 0.200 | 1 | 159054878 | missense variant | A/T | snv | 0.15 | 0.17 | 1 | |
| rs1327295035 | 1.000 | 0.200 | 6 | 52187730 | missense variant | A/G | snv | 1 | |||
| rs201890924 | 1.000 | 0.200 | 6 | 52187736 | missense variant | G/A | snv | 5.2E-05 | 2.8E-05 | 1 | |
| rs11574944 | 1.000 | 0.200 | 16 | 30498669 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs2929 | 1.000 | 0.200 | 16 | 31381987 | 3 prime UTR variant | G/A | snv | 0.28 | 1 | ||
| rs2256298 | 1.000 | 0.200 | 1 | 64864999 | intron variant | G/A | snv | 0.30 | 0.36 | 1 | |
| rs310245 | 1.000 | 0.200 | 1 | 64840499 | intron variant | C/T | snv | 0.51 | 1 | ||
| rs2617170 | 1.000 | 0.200 | 12 | 10408358 | missense variant | T/C | snv | 0.63 | 0.61 | 1 | |
| rs149034313 | 1.000 | 0.200 | 22 | 31278338 | missense variant | C/G;T | snv | 6.4E-03; 1.2E-05 | 1 | ||
| rs4489285 | 1.000 | 0.200 | 8 | 31540605 | intron variant | G/A | snv | 0.58 | 1 | ||
| rs1608157 | 1.000 | 0.200 | 7 | 150549936 | intergenic variant | C/G;T | snv | 1 | |||
| rs9368678 | 1.000 | 0.200 | 6 | 31304686 | intron variant | T/C | snv | 9.2E-02 | 1 | ||
| rs1057519328 | 1.000 | 0.200 | 16 | 3249592 | missense variant | G/C | snv | 2.1E-05 | 1 | ||
| rs751454741 | 1.000 | 0.200 | 16 | 3254736 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs755659290 | 1.000 | 0.200 | 16 | 3249480 | missense variant | T/C | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs3094584 | 1.000 | 0.200 | 6 | 31416071 | intron variant | G/A;T | snv | 0.17 | 1 | ||
| rs3093953 | 1.000 | 0.200 | 6 | 31506911 | intron variant | T/G | snv | 0.80 | 1 | ||
| rs3914501 | 1.000 | 0.200 | 3 | 174846878 | intron variant | A/G | snv | 0.21 | 1 |