| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28357984 | 0.851 | 0.160 | MT | 5178 | missense variant | C/A | snv | 6 | |||
| rs702553 | 0.882 | 0.160 | 5 | 60440946 | intron variant | A/T | snv | 0.37 | 6 | ||
| rs2075575 | 0.851 | 0.200 | 18 | 26866562 | intron variant | G/A | snv | 0.31 | 5 | ||
| rs779829591 | 0.827 | 0.320 | 1 | 94532395 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
| rs7522061 | 0.882 | 0.320 | 1 | 157698600 | missense variant | T/C;G | snv | 0.45 | 0.51 | 4 | |
| rs3805435 | 0.882 | 0.120 | 5 | 151021735 | non coding transcript exon variant | T/C | snv | 8.4E-02 | 3 | ||
| rs3840634 | 0.925 | 0.120 | 7 | 116556798 | intron variant | T/C | snv | 2 | |||
| rs3736309 | 0.925 | 0.120 | 12 | 49964271 | intron variant | A/G | snv | 0.12 | 2 | ||
| rs10489678 | 1.000 | 0.120 | 1 | 157699878 | intron variant | G/A;C;T | snv | 1 | |||
| rs10955255 | 1.000 | 0.120 | 8 | 101524177 | intron variant | A/G;T | snv | 1 | |||
| rs6989650 | 1.000 | 0.120 | 8 | 101669109 | 3 prime UTR variant | C/T | snv | 0.24 | 1 | ||
| rs611419 | 1.000 | 0.120 | 8 | 101491489 | intron variant | T/A;C | snv | 1 | |||
| rs1264525329 | 1.000 | 0.120 | 6 | 159682587 | missense variant | T/C | snv | 4.0E-06 | 1 |