| 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 | 34 | |
| rs2820443 | 0.882 | 0.120 | 1 | 219580167 | regulatory region variant | T/C | snv | 0.23 | 8 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 6 | ||
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 6 | |||
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 5 | |
| rs1333062 | 0.807 | 0.200 | 1 | 160876494 | downstream gene variant | T/C;G | snv | 5 | |||
| rs3768321 | 1.000 | 0.080 | 1 | 39570256 | intron variant | G/T | snv | 0.14 | 5 | ||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 4 | |
| rs2296172 | 1.000 | 0.080 | 1 | 39370145 | missense variant | A/G;T | snv | 0.19; 8.0E-06 | 4 | ||
| rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 4 | |||
| rs1892534 | 0.925 | 0.120 | 1 | 65640261 | 3 prime UTR variant | C/T | snv | 0.44 | 3 | ||
| rs2201841 | 0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv | 3 | |||
| rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 3 | ||
| rs6136 | 0.752 | 0.440 | 1 | 169594713 | missense variant | T/G | snv | 8.2E-02 | 7.5E-02 | 3 | |
| rs6662618 | 0.882 | 0.200 | 1 | 92469854 | downstream gene variant | T/G | snv | 0.75 | 3 | ||
| rs6700896 | 0.827 | 0.160 | 1 | 65624099 | intron variant | C/T | snv | 0.44 | 3 | ||
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 3 | |
| rs10911021 | 0.807 | 0.160 | 1 | 182112825 | intron variant | C/T | snv | 0.36 | 2 | ||
| rs11573156 | 0.882 | 0.240 | 1 | 19979653 | 5 prime UTR variant | G/C | snv | 0.19 | 2 | ||
| rs12040333 | 1.000 | 0.080 | 1 | 43848369 | intron variant | G/A;C | snv | 2 | |||
| rs17513135 | 1.000 | 0.080 | 1 | 39570014 | intron variant | C/A;T | snv | 0.17 | 0.16 | 2 | |
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 2 | ||
| rs181126208 | 1.000 | 0.080 | 1 | 236495210 | intron variant | G/A | snv | 4.9E-02 | 2 | ||
| rs2631781 | 1.000 | 0.080 | 1 | 76128101 | intron variant | C/A;T | snv | 2 |