| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12068753 | 1.000 | 0.120 | 1 | 159722747 | intergenic variant | T/A | snv | 0.15 | 2 | ||
| rs17667932 | 1.000 | 0.120 | 8 | 117537137 | intron variant | T/C | snv | 7.5E-02 | 2 | ||
| rs10082659 | 1.000 | 0.120 | 11 | 36122428 | intron variant | G/T | snv | 0.42 | 1 | ||
| rs10100215 | 1.000 | 0.120 | 8 | 11504763 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs10866845 | 1.000 | 0.120 | 8 | 25850751 | synonymous variant | T/C | snv | 0.42 | 0.49 | 1 | |
| rs1113452 | 1.000 | 0.120 | 15 | 82805465 | intron variant | G/A | snv | 3.5E-05 | 1 | ||
| rs11250141 | 1.000 | 0.120 | 8 | 11514632 | intron variant | G/A | snv | 0.48 | 1 | ||
| rs11340705 | 1.000 | 0.120 | 3 | 16526578 | intron variant | AA/-;A;AAA | delins | 1 | |||
| rs1150793 | 1.000 | 0.120 | 6 | 31749919 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs11734 | 1.000 | 0.120 | 7 | 99632145 | 3 prime UTR variant | G/A;C | snv | 1 | |||
| rs11990277 | 1.000 | 0.120 | 8 | 11514576 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs12722477 | 1.000 | 0.120 | 6 | 29828599 | missense variant | C/A | snv | 0.14 | 0.14 | 1 | |
| rs13256690 | 1.000 | 0.120 | 8 | 11481059 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs1438386 | 1.000 | 0.120 | 15 | 67115561 | intron variant | G/A | snv | 0.51 | 1 | ||
| rs1478887 | 1.000 | 0.120 | 8 | 11498471 | intron variant | C/T | snv | 0.64 | 1 | ||
| rs1478895 | 1.000 | 0.120 | 8 | 11495826 | intron variant | G/C | snv | 0.83 | 1 | ||
| rs1478900 | 1.000 | 0.120 | 8 | 11490151 | intron variant | C/G;T | snv | 1 | |||
| rs1478901 | 1.000 | 0.120 | 8 | 11490324 | intron variant | G/C | snv | 0.25 | 1 | ||
| rs1531577 | 1.000 | 0.120 | 8 | 11481052 | non coding transcript exon variant | C/T | snv | 0.71 | 1 | ||
| rs1585729 | 1.000 | 0.120 | 8 | 11502536 | intron variant | G/C | snv | 0.44 | 1 | ||
| rs16849083 | 1.000 | 0.120 | 3 | 139465437 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs17161726 | 1.000 | 0.120 | 7 | 99410772 | intron variant | C/G | snv | 7.8E-02 | 1 | ||
| rs17280682 | 1.000 | 0.120 | 11 | 7070338 | missense variant | C/T | snv | 0.15 | 0.15 | 1 | |
| rs17416878 | 1.000 | 0.120 | 1 | 16120485 | downstream gene variant | A/G | snv | 0.24 | 1 | ||
| rs17531088 | 1.000 | 0.120 | 3 | 175175985 | intron variant | C/T | snv | 0.34 | 1 |