| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17111684 | 1 | 55159875 | intron variant | C/T | snv | 3.8E-02 | 3 | ||||
| rs191448950 | 1 | 55119171 | intron variant | G/A | snv | 6.4E-03 | 3 | ||||
| rs193084249 | 1 | 26661155 | intergenic variant | A/G | snv | 1.7E-02 | 3 | ||||
| rs2131925 | 1 | 62560271 | intron variant | G/T | snv | 0.57 | 3 | ||||
| rs3850634 | 1 | 62584927 | intron variant | T/G | snv | 0.33 | 0.34 | 3 | |||
| rs3902354 | 1 | 109276674 | downstream gene variant | C/A;T | snv | 3 | |||||
| rs602633 | 0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 | 3 | ||
| rs6587980 | 1 | 62625187 | synonymous variant | C/T | snv | 0.40 | 3 | ||||
| rs660240 | 1 | 109275216 | 3 prime UTR variant | T/C | snv | 0.75 | 3 | ||||
| rs661955 | 1 | 234707109 | upstream gene variant | G/C;T | snv | 3 | |||||
| rs6657811 | 1 | 109264661 | intron variant | A/C;T | snv | 4.0E-06; 0.10 | 3 | ||||
| rs7544735 | 1.000 | 0.040 | 1 | 220825571 | intron variant | G/A | snv | 0.22 | 3 | ||
| rs995000 | 1 | 62641855 | intron variant | C/T | snv | 0.34 | 3 | ||||
| rs9988450 | 1 | 62458777 | non coding transcript exon variant | C/T | snv | 0.39 | 3 | ||||
| rs11164654 | 1 | 92502755 | regulatory region variant | T/C | snv | 0.85 | 2 | ||||
| rs11806638 | 1 | 55052487 | intron variant | C/A;G | snv | 2 | |||||
| rs12027135 | 1 | 25449242 | intron variant | A/T | snv | 0.50 | 2 | ||||
| rs12117661 | 1 | 55021673 | downstream gene variant | C/G | snv | 0.28 | 2 | ||||
| rs145955280 | 1 | 92671973 | intron variant | A/-;AA;AAA | delins | 2 | |||||
| rs147943615 | 1 | 55902364 | intron variant | A/G;T | snv | 2 | |||||
| rs151193009 | 1 | 55043912 | missense variant | C/T | snv | 7.4E-04 | 1.5E-04 | 2 | |||
| rs17111503 | 0.925 | 0.160 | 1 | 55037775 | upstream gene variant | A/G | snv | 0.22 | 2 | ||
| rs1730859 | 1 | 107075085 | intergenic variant | G/A | snv | 0.75 | 2 | ||||
| rs1874124 | 1 | 220801995 | intron variant | C/T | snv | 0.11 | 2 | ||||
| rs2027061 | 1 | 92535873 | intron variant | C/T | snv | 0.85 | 2 |