| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7815944 | 1.000 | 0.120 | 8 | 128415272 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs10995251 | 1.000 | 0.120 | 10 | 62638706 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs9368677 | 1.000 | 0.120 | 6 | 31304544 | intron variant | G/A | snv | 7.4E-02 | 1 | ||
| rs55879323 | 1.000 | 0.120 | 1 | 152196264 | intron variant | C/T | snv | 0.42 | 1 | ||
| rs370555009 | 1.000 | 0.120 | 5 | 179794090 | missense variant | G/A;C | snv | 1.6E-05; 4.0E-06 | 1 | ||
| rs6686734 | 1.000 | 0.120 | 1 | 12008884 | intron variant | T/C | snv | 0.71 | 1 | ||
| rs2271404 | 1.000 | 0.120 | 2 | 111246290 | non coding transcript exon variant | T/C | snv | 0.12 | 1 | ||
| rs17173197 | 1.000 | 0.120 | 7 | 151571834 | non coding transcript exon variant | C/T | snv | 0.34 | 1 | ||
| rs2592555 | 1.000 | 0.120 | 11 | 36350207 | intron variant | T/C;G | snv | 1 | |||
| rs4643526 | 1.000 | 0.120 | 2 | 60957516 | intron variant | G/A | snv | 0.35 | 1 | ||
| rs2897443 | 1.000 | 0.120 | 5 | 132593902 | intron variant | G/T | snv | 0.18 | 1 | ||
| rs1665050 | 1.000 | 0.120 | 15 | 59001406 | intron variant | A/G;T | snv | 1 | |||
| rs909341 | 1.000 | 0.120 | 20 | 63697389 | synonymous variant | C/T | snv | 0.25 | 0.19 | 1 | |
| rs4809219 | 1.000 | 0.120 | 20 | 63671762 | intron variant | C/A;G;T | snv | 1 | |||
| rs17881320 | 1.000 | 0.120 | 17 | 42333221 | intron variant | G/A;T | snv | 6.0E-02 | 1 | ||
| rs9050 | 1.000 | 0.120 | 1 | 152106838 | 3 prime UTR variant | C/A | snv | 4.3E-02 | 1 | ||
| rs12188917 | 1.000 | 0.120 | 5 | 132655393 | intron variant | T/C;G | snv | 1 | |||
| rs10067777 | 1.000 | 0.120 | 5 | 110490595 | intron variant | A/G | snv | 7.4E-02 | 1 | ||
| rs7701890 | 1.000 | 0.120 | 5 | 110523120 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs41268896 | 1.000 | 0.120 | 6 | 32102292 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs9469099 | 1.000 | 0.120 | 6 | 32341131 | intron variant | G/A;T | snv | 1 | |||
| rs6720763 | 1.000 | 0.120 | 2 | 167135776 | intron variant | T/C | snv | 0.27 | 1 | ||
| rs512685 | 1.000 | 0.120 | 6 | 149471889 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs2393903 | 1.000 | 0.120 | 10 | 62620576 | intron variant | T/A;C | snv | 1 | |||
| rs112111458 | 0.925 | 0.120 | 2 | 70872975 | intergenic variant | A/G | snv | 0.16 | 2 |