| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1408579 | 1.000 | 0.040 | 10 | 100152437 | intron variant | C/T | snv | 0.32 | 3 | ||
| rs7157599 | 0.925 | 0.040 | 14 | 100159565 | missense variant | C/T | snv | 0.73 | 0.76 | 6 | |
| rs6712515 | 0.925 | 0.160 | 2 | 100190052 | intron variant | T/A;C | snv | 3 | |||
| rs117304774 | 1.000 | 0.040 | 16 | 10057377 | intron variant | G/A | snv | 8.2E-03 | 2 | ||
| rs221798 | 0.882 | 0.040 | 7 | 100689872 | intron variant | C/A;G | snv | 3 | |||
| rs221780 | 1.000 | 0.040 | 7 | 100699412 | regulatory region variant | G/C;T | snv | 2 | |||
| rs221774 | 0.851 | 0.080 | 7 | 100701361 | upstream gene variant | A/G;T | snv | 4 | |||
| rs506597 | 0.882 | 0.040 | 7 | 100715797 | upstream gene variant | A/G | snv | 0.90 | 4 | ||
| rs1734907 | 0.925 | 0.080 | 7 | 100717894 | upstream gene variant | A/G | snv | 0.84 | 4 | ||
| rs7214058 | 1.000 | 0.040 | 17 | 10080017 | intron variant | T/A;G | snv | 2 | |||
| rs644939 | 1.000 | 0.040 | 12 | 101060211 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs13096071 | 1.000 | 0.040 | 3 | 101082799 | intergenic variant | T/A;C | snv | 1 | |||
| rs9518320 | 1.000 | 0.040 | 13 | 101167478 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs9518331 | 1.000 | 0.040 | 13 | 101173903 | intron variant | G/T | snv | 0.25 | 1 | ||
| rs2114724 | 1.000 | 0.040 | 19 | 10154572 | intron variant | T/C | snv | 0.52 | 0.51 | 1 | |
| rs2228611 | 0.708 | 0.520 | 19 | 10156401 | synonymous variant | T/A;C | snv | 0.52 | 19 | ||
| rs114540395 | 1.000 | 0.040 | 10 | 101719305 | intron variant | C/T | snv | 9.2E-02 | 1 | ||
| rs73191547 | 1.000 | 0.040 | 8 | 10175915 | intron variant | A/T | snv | 0.28 | 2 | ||
| rs782803949 | 1.000 | 0.040 | 7 | 102178612 | synonymous variant | C/T | snv | 1.4E-05 | 1 | ||
| rs6039769 | 1.000 | 0.040 | 20 | 10218306 | intron variant | A/C;G | snv | 1 | |||
| rs782679604 | 1.000 | 0.040 | 7 | 102189836 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs6855246 | 1.000 | 0.040 | 4 | 102191313 | intergenic variant | A/G | snv | 0.14 | 4 | ||
| rs35225200 | 1.000 | 0.040 | 4 | 102225731 | intergenic variant | A/C | snv | 5.4E-02 | 5 | ||
| rs35518360 | 1.000 | 0.040 | 4 | 102225733 | intergenic variant | A/G;T | snv | 1 | |||
| rs4919621 | 0.851 | 0.080 | 10 | 102238914 | intron variant | A/T | snv | 0.66 | 4 |