| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1874564 | 0.925 | 0.080 | 4 | 76936952 | intergenic variant | G/A | snv | 0.58 | 2 | ||
| rs2286742 | 1.000 | 0.080 | 10 | 113580733 | intron variant | G/A;C | snv | 0.57; 8.2E-06 | 2 | ||
| rs33954691 | 1.000 | 0.080 | 5 | 1255405 | synonymous variant | G/A | snv | 0.13 | 9.0E-02 | 2 | |
| rs368187 | 0.925 | 0.080 | 14 | 36063370 | non coding transcript exon variant | G/A;C;T | snv | 2 | |||
| rs3740530 | 1.000 | 0.080 | 10 | 113574365 | synonymous variant | C/T | snv | 0.63 | 0.55 | 2 | |
| rs377767394 | 0.925 | 0.080 | 10 | 43113603 | missense variant | A/C | snv | 2 | |||
| rs4461062 | 1.000 | 0.080 | 16 | 56830706 | intron variant | C/T | snv | 0.48 | 0.48 | 2 | |
| rs4649295 | 0.925 | 0.080 | 1 | 233280792 | intron variant | T/C | snv | 0.60 | 2 | ||
| rs62054619 | 1.000 | 0.080 | 16 | 90029890 | non coding transcript exon variant | G/A | snv | 0.14 | 2 | ||
| rs6996585 | 0.925 | 0.080 | 8 | 32543285 | intron variant | A/G | snv | 0.37 | 2 | ||
| rs782237788 | 1.000 | 0.080 | 10 | 46009499 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs864622088 | 0.925 | 0.080 | 9 | 95459774 | missense variant | G/T | snv | 4.0E-06 | 2 | ||
| rs9858271 | 0.925 | 0.080 | 3 | 59559604 | intron variant | G/A | snv | 0.80 | 2 | ||
| rs10119760 | 1.000 | 0.080 | 9 | 97862320 | intergenic variant | G/C;T | snv | 1 | |||
| rs1025689 | 1.000 | 0.080 | 3 | 53849695 | synonymous variant | C/A;G;T | snv | 8.0E-06; 0.56 | 1 | ||
| rs1061758 | 1.000 | 0.080 | 9 | 34652333 | intron variant | A/G | snv | 0.76 | 1 | ||
| rs1267636 | 1.000 | 0.080 | 7 | 140792239 | intron variant | T/C | snv | 0.11 | 1 | ||
| rs1319984849 | 1.000 | 0.080 | 17 | 42727721 | frameshift variant | G/- | delins | 1 | |||
| rs1394069156 | 1.000 | 0.080 | 22 | 28703554 | missense variant | T/G | snv | 1 | |||
| rs144110687 | 1.000 | 0.080 | 22 | 21025856 | synonymous variant | C/G;T | snv | 4.3E-05 | 1 | ||
| rs1466683466 | 1.000 | 0.080 | 11 | 57348630 | synonymous variant | C/T | snv | 1 | |||
| rs1467664274 | 1.000 | 0.080 | 22 | 28695186 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1486830727 | 1.000 | 0.080 | 4 | 147532671 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs149019598 | 1.000 | 0.080 | 16 | 2761565 | missense variant | C/T | snv | 5.7E-04 | 7.1E-04 | 1 | |
| rs149959485 | 1.000 | 0.080 | 3 | 45947356 | missense variant | G/T | snv | 4.0E-06 | 1 |