| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 9 | |||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
| rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 5 | |||
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 4 | ||
| rs2201841 | 0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv | 4 | |||
| rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 4 | ||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 3 | |
| rs10923931 | 0.925 | 0.120 | 1 | 119975336 | intron variant | G/T | snv | 0.17 | 2 | ||
| rs3093059 | 0.752 | 0.520 | 1 | 159715346 | upstream gene variant | A/G | snv | 0.13 | 2 | ||
| rs3806185 | 1.000 | 0.080 | 1 | 159779096 | upstream gene variant | C/T | snv | 0.14 | 2 | ||
| rs1027700 | 1.000 | 0.080 | 1 | 161787246 | intron variant | A/T | snv | 0.21 | 1 | ||
| rs10494366 | 0.851 | 0.200 | 1 | 162115895 | intron variant | G/T | snv | 0.54 | 1 | ||
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 1 | |
| rs1150253 | 1.000 | 0.080 | 1 | 206898250 | intron variant | G/A;C | snv | 1 | |||
| rs1150256 | 0.925 | 0.120 | 1 | 206899788 | intron variant | G/A | snv | 0.40 | 1 | ||
| rs1150258 | 1.000 | 0.080 | 1 | 206901560 | missense variant | T/A;C;G | snv | 0.40 | 0.40 | 1 | |
| rs11576878 | 1.000 | 0.080 | 1 | 161805787 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs11581556 | 1.000 | 0.080 | 1 | 161823822 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs1193179 | 1.000 | 0.080 | 1 | 7509542 | intron variant | C/T | snv | 0.62 | 1 | ||
| rs12027542 | 1.000 | 0.080 | 1 | 233204408 | intron variant | A/G | snv | 6.6E-02 | 1 | ||
| rs12143842 | 0.925 | 0.160 | 1 | 162064100 | intergenic variant | C/T | snv | 0.22 | 1 | ||
| rs1342061 | 1.000 | 0.080 | 1 | 205942257 | intron variant | T/A;G | snv | 1 | |||
| rs1342063 | 1.000 | 0.080 | 1 | 205943731 | upstream gene variant | C/T | snv | 0.37 | 1 | ||
| rs1342064 | 1.000 | 0.080 | 1 | 205943945 | upstream gene variant | T/C | snv | 0.36 | 1 |