| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 9 | ||
| rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 8 | ||
| rs13118928 | 0.925 | 0.040 | 4 | 144565237 | intron variant | A/G | snv | 0.33 | 7 | ||
| rs7655625 | 1.000 | 0.040 | 4 | 144564763 | intron variant | T/C;G | snv | 7 | |||
| rs7671167 | 0.925 | 0.040 | 4 | 88962828 | intron variant | C/T | snv | 0.53 | 7 | ||
| rs12504628 | 1.000 | 0.040 | 4 | 144515172 | intron variant | T/C | snv | 0.33 | 6 | ||
| rs1529672 | 1.000 | 0.040 | 3 | 25479091 | intron variant | C/A;T | snv | 6 | |||
| rs9788721 | 1.000 | 0.040 | 15 | 78510527 | intron variant | C/T | snv | 0.65 | 6 | ||
| rs138544659 | 1.000 | 0.040 | 15 | 78608359 | intron variant | T/G | snv | 0.28 | 5 | ||
| rs1512288 | 1.000 | 0.040 | 4 | 144570129 | intron variant | G/A | snv | 0.42 | 5 | ||
| rs1828591 | 1.000 | 0.040 | 4 | 144559628 | intron variant | A/G | snv | 0.43 | 5 | ||
| rs2013701 | 1.000 | 0.040 | 4 | 88963935 | intron variant | G/T | snv | 0.51 | 5 | ||
| rs34651 | 1.000 | 0.040 | 5 | 72848178 | non coding transcript exon variant | C/T | snv | 0.94 | 5 | ||
| rs34712979 | 1.000 | 0.040 | 4 | 105897896 | splice region variant | G/A;T | snv | 0.17 | 5 | ||
| rs3995090 | 1.000 | 0.040 | 5 | 148466252 | intron variant | A/C | snv | 0.39 | 5 | ||
| rs55958997 | 1.000 | 0.040 | 15 | 78623530 | upstream gene variant | C/A | snv | 0.32 | 5 | ||
| rs6817273 | 1.000 | 0.040 | 4 | 144570851 | intron variant | T/A;C | snv | 0.33 | 5 | ||
| rs6830970 | 1.000 | 0.040 | 4 | 88855930 | 3 prime UTR variant | A/G | snv | 0.38 | 5 | ||
| rs7068966 | 1.000 | 0.040 | 10 | 12235993 | intron variant | C/T | snv | 0.43 | 5 | ||
| rs7697189 | 1.000 | 0.040 | 4 | 144515742 | intron variant | G/A;C | snv | 5 | |||
| rs7733088 | 1.000 | 0.040 | 5 | 148476770 | intron variant | G/A;C | snv | 0.44; 4.1E-06 | 5 | ||
| rs8031948 | 1.000 | 0.040 | 15 | 78523715 | intron variant | G/T | snv | 0.27 | 5 | ||
| rs153916 | 1.000 | 0.040 | 5 | 95700996 | upstream gene variant | C/A;G;T | snv | 4 | |||
| rs17484524 | 1.000 | 0.040 | 15 | 78480334 | intron variant | A/G | snv | 0.23 | 4 | ||
| rs17487223 | 1.000 | 0.040 | 15 | 78631645 | intron variant | C/T | snv | 0.27 | 4 |