| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057941 | 0.701 | 0.280 | 1 | 155216951 | non coding transcript exon variant | G/A;T | snv | 0.46 | 18 | ||
| rs11119608 | 0.708 | 0.280 | 1 | 210816167 | intron variant | T/G | snv | 0.21 | 17 | ||
| rs186507655 | 0.708 | 0.280 | 1 | 1351675 | upstream gene variant | G/A | snv | 6.8E-03 | 17 | ||
| rs2974935 | 0.708 | 0.280 | 1 | 155212052 | non coding transcript exon variant | G/A;C;T | snv | 17 | |||
| rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 14 | ||
| rs34612342 | 0.653 | 0.400 | 1 | 45332803 | missense variant | T/C | snv | 1.5E-03 | 1.6E-03 | 11 | |
| rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 9 | |
| rs36053993 | 0.677 | 0.280 | 1 | 45331556 | missense variant | C/T | snv | 3.0E-03 | 3.3E-03 | 9 | |
| rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 8 | |
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 8 | ||
| rs121913121 | 0.851 | 0.320 | 1 | 241513661 | missense variant | T/G | snv | 6 | |||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 6 | |
| rs4245739 | 0.708 | 0.360 | 1 | 204549714 | 3 prime UTR variant | C/A;G | snv | 0.77; 6.2E-06 | 6 | ||
| rs2235544 | 0.742 | 0.240 | 1 | 53909897 | intron variant | C/A;T | snv | 0.53; 4.0E-06 | 4 | ||
| rs301806 | 0.851 | 0.120 | 1 | 8422018 | intron variant | C/T | snv | 0.62 | 4 | ||
| rs4971059 | 0.851 | 0.200 | 1 | 155176305 | intron variant | G/A | snv | 0.34 | 4 | ||
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 4 | |
| rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 3 | |||
| rs12405132 | 0.882 | 0.200 | 1 | 145790097 | intron variant | G/A | snv | 0.29 | 3 | ||
| rs72755295 | 1.000 | 0.080 | 1 | 241870961 | intron variant | A/G | snv | 2.1E-02 | 3 | ||
| rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 | ||
| rs11552449 | 0.925 | 0.080 | 1 | 113905767 | missense variant | C/G;T | snv | 0.22 | 0.15 | 2 | |
| rs17020562 | 0.925 | 0.080 | 1 | 213369363 | intergenic variant | T/C | snv | 5.9E-02 | 2 | ||
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 2 | ||
| rs4342822 | 0.882 | 0.080 | 1 | 213850882 | intron variant | G/T | snv | 0.62 | 2 |