| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1643821 | 6 | 151862416 | intron variant | G/A | snv | 0.46 | 2 | ||||
| rs10458894 | 11 | 3892042 | intron variant | T/A;C | snv | 1 | |||||
| rs11466414 | 14 | 75981507 | non coding transcript exon variant | G/A | snv | 4.7E-02 | 1 | ||||
| rs12710567 | X | 116170599 | upstream gene variant | T/C | snv | 3.2E-02 | 1 | ||||
| rs7945554 | 11 | 3857748 | intron variant | G/A | snv | 0.37 | 1 | ||||
| rs988328 | 6 | 151920015 | intron variant | T/C | snv | 0.15 | 1 | ||||
| rs41511344 | 0.882 | 0.040 | 4 | 148152550 | stop gained | G/A;T | snv | 5 | |||
| rs2234681 | 1.000 | 0.040 | 20 | 46008773 | upstream gene variant | ACACACACACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACACAC;ACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACACAC | delins | 2 | |||
| rs2235543 | 0.925 | 0.080 | 1 | 209687323 | intron variant | T/A;C | snv | 4 | |||
| rs3801266 | 0.925 | 0.080 | 7 | 106283804 | intron variant | T/C | snv | 0.26 | 3 | ||
| rs142724505 | 1.000 | 0.080 | 8 | 144080528 | missense variant | G/A | snv | 1.8E-03 | 1.7E-03 | 2 | |
| rs757574299 | 1.000 | 0.080 | 1 | 65570511 | missense variant | C/G | snv | 1.6E-05 | 1.4E-05 | 2 | |
| rs2881766 | 0.882 | 0.120 | 6 | 151797984 | intron variant | T/G | snv | 0.35 | 5 | ||
| rs1319501 | 0.882 | 0.120 | 7 | 106285307 | intron variant | C/A;T | snv | 0.76 | 4 | ||
| rs370402227 | 0.925 | 0.120 | 7 | 150996443 | missense variant | G/A;C | snv | 1.1E-05 | 4 | ||
| rs2016347 | 0.790 | 0.160 | 15 | 98960571 | 3 prime UTR variant | G/A;T | snv | 9 | |||
| rs2074192 | 0.827 | 0.160 | X | 15564667 | intron variant | C/T | snv | 0.40 | 9 | ||
| rs846910 | 0.882 | 0.160 | 1 | 209701909 | intron variant | A/G | snv | 0.95 | 6 | ||
| rs2070584 | 0.790 | 0.200 | X | 47587120 | intron variant | T/G | snv | 0.44 | 8 | ||
| rs2779249 | 0.851 | 0.200 | 17 | 27801555 | intron variant | C/A | snv | 0.33 | 7 | ||
| rs1177506410 | 0.776 | 0.240 | 1 | 230706148 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 12 | |
| rs1275805226 | 0.776 | 0.240 | 1 | 230706148 | frameshift variant | G/- | del | 7.0E-06 | 12 | ||
| rs3957357 | 0.807 | 0.280 | 6 | 52803889 | upstream gene variant | A/G | snv | 0.63 | 7 | ||
| rs6471 | 0.683 | 0.360 | 6 | 32040110 | missense variant | G/A;C;T | snv | 1.2E-05; 5.3E-03 | 24 | ||
| rs2740574 | 0.807 | 0.360 | 7 | 99784473 | upstream gene variant | C/T | snv | 0.78 | 12 |