| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs147856773 | 1.000 | 0.040 | 6 | 108666024 | intron variant | -/GGT | delins | 0.14 | 1 | ||
| rs17780256 | 0.827 | 0.120 | 17 | 72646784 | 3 prime UTR variant | A/C | snv | 0.18 | 6 | ||
| rs10775412 | 0.827 | 0.120 | 17 | 27542007 | intron variant | A/C | snv | 0.30 | 5 | ||
| rs1551399 | 0.827 | 0.120 | 8 | 125527723 | intron variant | A/C | snv | 0.46 | 5 | ||
| rs61802846 | 0.827 | 0.120 | 1 | 161504083 | upstream gene variant | A/C | snv | 8.8E-02 | 5 | ||
| rs1517352 | 0.851 | 0.160 | 2 | 191066738 | intron variant | A/C | snv | 0.45 | 3 | ||
| rs2382817 | 0.925 | 0.040 | 2 | 218286495 | 5 prime UTR variant | A/C | snv | 0.61 | 3 | ||
| rs7165170 | 1.000 | 0.040 | 15 | 90638257 | non coding transcript exon variant | A/C | snv | 0.26 | 2 | ||
| rs9891119 | 0.882 | 0.120 | 17 | 42355962 | intron variant | A/C | snv | 0.36 | 2 | ||
| rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 1 | ||
| rs11167764 | 0.925 | 0.120 | 5 | 142099500 | regulatory region variant | A/C | snv | 0.80 | 1 | ||
| rs140068907 | 1.000 | 0.040 | 6 | 32691666 | regulatory region variant | A/C | snv | 3.4E-03 | 1 | ||
| rs3763313 | 0.807 | 0.320 | 6 | 32408694 | upstream gene variant | A/C | snv | 0.21 | 1 | ||
| rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 7 | ||
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 7 | ||
| rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 7 | ||
| rs714830 | 0.827 | 0.120 | 6 | 20624151 | intron variant | A/C;G | snv | 0.13 | 5 | ||
| rs7195296 | 0.827 | 0.120 | 16 | 11655918 | intergenic variant | A/C;G | snv | 5 | |||
| rs10051722 | 1.000 | 0.040 | 5 | 130768383 | intron variant | A/C;G | snv | 2 | |||
| rs11871801 | 1.000 | 0.040 | 17 | 42418754 | intron variant | A/C;G | snv | 1 | |||
| rs1199103 | 1.000 | 0.040 | 10 | 58187470 | downstream gene variant | A/C;G | snv | 1 | |||
| rs2302759 | 1.000 | 0.040 | 16 | 50793690 | intron variant | A/C;G | snv | 4.0E-06; 0.79 | 1 | ||
| rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 1 | ||
| rs7076156 | 0.925 | 0.120 | 10 | 62655424 | missense variant | A/C;G | snv | 0.80 | 1 | ||
| rs740495 | 1.000 | 0.040 | 19 | 1124836 | intron variant | A/C;G | snv | 1 |