| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 27 | ||
| rs12392447 | 1.000 | 0.080 | X | 154496001 | non coding transcript exon variant | A/G | snv | 1 | |||
| rs12427267 | 1.000 | 0.080 | 12 | 91930196 | intergenic variant | A/G | snv | 0.49 | 1 | ||
| rs12482570 | 1.000 | 0.080 | 21 | 37705475 | intron variant | A/G | snv | 0.30 | 3 | ||
| rs12489456 | 1.000 | 0.080 | 3 | 14459666 | intron variant | G/A;T | snv | 1 | |||
| rs12544026 | 0.925 | 0.080 | 8 | 101819970 | intron variant | G/A | snv | 0.85 | 4 | ||
| rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 64 | |
| rs12639833 | 1.000 | 0.080 | 4 | 99346215 | intron variant | C/T | snv | 0.31 | 3 | ||
| rs12898370 | 1.000 | 0.080 | 15 | 77516256 | intergenic variant | A/C;T | snv | 3 | |||
| rs12898460 | 0.882 | 0.080 | 15 | 38694612 | intron variant | C/T | snv | 0.23 | 3 | ||
| rs12901215 | 1.000 | 0.080 | 15 | 38700692 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs12903120 | 1.000 | 0.080 | 15 | 38695896 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs12912251 | 0.882 | 0.080 | 15 | 38694167 | intron variant | G/T | snv | 0.25 | 3 | ||
| rs12916379 | 1.000 | 0.080 | 15 | 38699319 | non coding transcript exon variant | A/G | snv | 0.22 | 1 | ||
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 30 | ||
| rs1316543 | 1.000 | 0.080 | 10 | 119445148 | intron variant | G/A | snv | 0.15 | 3 | ||
| rs137852569 | 0.752 | 0.320 | X | 67686030 | missense variant | G/A | snv | 9.4E-06 | 3 | ||
| rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 4 | ||
| rs1399590 | 1.000 | 0.080 | 21 | 37681768 | intron variant | G/A | snv | 0.56 | 3 | ||
| rs1399591 | 1.000 | 0.080 | 21 | 37681654 | intron variant | C/T | snv | 0.50 | 3 | ||
| rs1399592 | 1.000 | 0.080 | 21 | 37681559 | intron variant | T/A;G | snv | 0.52 | 3 | ||
| rs141424017 | 1.000 | 0.080 | 7 | 115311376 | intergenic variant | -/CAA | ins | 3 | |||
| rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 16 | ||
| rs1437396 | 1.000 | 0.080 | 2 | 55278320 | upstream gene variant | C/G;T | snv | 3 | |||
| rs143894582 | 1.000 | 0.080 | 12 | 112469070 | intron variant | A/-;AA | delins | 1 |