| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10835920 | 1.000 | 0.080 | 11 | 32468118 | intergenic variant | C/T | snv | 0.50 | 1 | ||
| rs113998067 | 1.000 | 0.080 | 1 | 37607755 | downstream gene variant | T/C | snv | 3.3E-02 | 1 | ||
| rs11583244 | 1.000 | 0.080 | 1 | 225764772 | regulatory region variant | C/T | snv | 0.35 | 1 | ||
| rs117280150 | 1.000 | 0.080 | 8 | 14014030 | intergenic variant | T/G | snv | 2.3E-02 | 1 | ||
| rs11841589 | 1.000 | 0.080 | 13 | 73240754 | intergenic variant | G/T | snv | 0.31 | 1 | ||
| rs148261157 | 1.000 | 0.080 | 2 | 60670444 | intergenic variant | G/A | snv | 3.9E-02 | 1 | ||
| rs1679014 | 1.000 | 0.080 | 9 | 22207038 | intron variant | T/A;C | snv | 1 | |||
| rs370989584 | 1.000 | 0.080 | 4 | 133040031 | intergenic variant | T/- | del | 8.8E-03 | 1 | ||
| rs376674848 | 1.000 | 0.080 | 12 | 84220725 | intron variant | -/ATGTGT | delins | 1 | |||
| rs4052756 | 1.000 | 0.080 | 6 | 19914263 | intergenic variant | C/T | snv | 0.55 | 1 | ||
| rs4733613 | 1.000 | 0.080 | 8 | 128587032 | intergenic variant | C/G | snv | 0.86 | 1 | ||
| rs571866661 | 1.000 | 0.080 | 11 | 77315297 | downstream gene variant | TTTTTTTTTTTTTTTTT/-;T;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT | delins | 8.7E-02 | 1 | ||
| rs7981863 | 1.000 | 0.080 | 13 | 73238004 | intergenic variant | C/T | snv | 0.32 | 1 | ||
| rs8176323 | 1.000 | 0.080 | 17 | 43043694 | downstream gene variant | G/C | snv | 0.31 | 1 | ||
| rs9600103 | 1.000 | 0.080 | 13 | 73237742 | intergenic variant | A/T | snv | 0.33 | 1 | ||
| rs2498796 | 1.000 | 0.080 | 14 | 104776883 | non coding transcript exon variant | G/A | snv | 0.33 | 1 | ||
| rs911162 | 1.000 | 0.080 | 20 | 56391393 | intron variant | A/C;G | snv | 1 | |||
| rs60856912 | 1.000 | 0.080 | 17 | 67896227 | intron variant | G/T | snv | 0.32 | 1 | ||
| rs2070833 | 1.000 | 0.080 | 17 | 43090832 | intron variant | G/T | snv | 2.1E-02 | 1 | ||
| rs8067269 | 1.000 | 0.080 | 17 | 43083782 | intron variant | G/A | snv | 0.52 | 1 | ||
| rs8176199 | 1.000 | 0.080 | 17 | 43078507 | intron variant | T/G | snv | 0.23 | 1 | ||
| rs6499199 | 1.000 | 0.080 | 16 | 68815934 | intron variant | C/T | snv | 0.14 | 1 | ||
| rs17761446 | 1.000 | 0.080 | 9 | 22118103 | non coding transcript exon variant | T/G | snv | 2.0E-02 | 1 | ||
| rs9639594 | 1.000 | 0.080 | 7 | 29139570 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs79024726 | 1.000 | 0.080 | 1 | 33832760 | intron variant | T/A;G | snv | 1 |