| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2280141 | 1.000 | 0.040 | 10 | 122433665 | 3 prime UTR variant | T/G | snv | 0.56 | 1 | ||
| rs7072204 | 0.925 | 0.120 | 10 | 122435969 | 3 prime UTR variant | A/G | snv | 0.47 | 1 | ||
| rs10490924 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 4 | |
| rs3750848 | 1.000 | 0.040 | 10 | 122455799 | intron variant | T/G | snv | 0.23 | 1 | ||
| rs3750846 | 0.851 | 0.040 | 10 | 122456049 | intron variant | T/C | snv | 0.24 | 4 | ||
| rs3793917 | 0.882 | 0.040 | 10 | 122459759 | non coding transcript exon variant | C/G | snv | 0.23 | 1 | ||
| rs11200638 | 0.724 | 0.280 | 10 | 122461028 | non coding transcript exon variant | G/A | snv | 0.23 | 3 | ||
| rs2284665 | 0.882 | 0.040 | 10 | 122467114 | intron variant | G/A;T | snv | 3 | |||
| rs10191751 | 1.000 | 0.040 | 2 | 12822189 | intron variant | A/G;T | snv | 0.68 | 1 | ||
| rs154001 | 1.000 | 0.040 | 5 | 128349443 | missense variant | C/G;T | snv | 0.73 | 2 | ||
| rs8177179 | 0.925 | 0.080 | 3 | 133744613 | intron variant | G/A | snv | 0.58 | 2 | ||
| rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 1 | ||
| rs2842992 | 0.925 | 0.040 | 6 | 159650127 | intron variant | G/A | snv | 0.73 | 1 | ||
| rs1800947 | 0.683 | 0.440 | 1 | 159713648 | splice region variant | C/A;G;T | snv | 4.4E-05; 5.1E-02; 4.0E-06 | 1 | ||
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 7 | ||
| rs1136287 | 0.790 | 0.280 | 17 | 1769982 | missense variant | C/T | snv | 0.61 | 0.69 | 1 | |
| rs187328863 | 0.851 | 0.040 | 1 | 196411028 | intron variant | C/T | snv | 1.6E-02 | 4 | ||
| rs4657825 | 1.000 | 0.040 | 1 | 196615191 | intergenic variant | A/G;T | snv | 1 | |||
| rs12061508 | 1.000 | 0.040 | 1 | 196615338 | intergenic variant | G/A | snv | 0.23 | 1 | ||
| rs148553336 | 0.851 | 0.040 | 1 | 196644043 | intergenic variant | T/C | snv | 7.7E-03 | 4 | ||
| rs3753394 | 0.882 | 0.040 | 1 | 196651787 | upstream gene variant | C/T | snv | 0.22 | 1 | ||
| rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 5 | |
| rs1329424 | 1.000 | 0.040 | 1 | 196677046 | non coding transcript exon variant | T/G | snv | 0.66 | 1 | ||
| rs1061147 | 1.000 | 0.040 | 1 | 196685194 | synonymous variant | A/C | snv | 0.68 | 0.62 | 1 | |
| rs10801553 | 1.000 | 0.040 | 1 | 196686613 | intron variant | A/C | snv | 0.64 | 1 |