| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs174577 | 1.000 | 0.080 | 11 | 61837342 | intron variant | C/A | snv | 0.38 | 13 | ||
| rs1996371 | 1.000 | 0.080 | 15 | 78664464 | intron variant | T/C | snv | 0.28 | 4 | ||
| rs4887077 | 1.000 | 0.080 | 15 | 78686022 | intron variant | C/T | snv | 0.28 | 4 | ||
| rs174534 | 1.000 | 0.080 | 11 | 61781986 | non coding transcript exon variant | A/G | snv | 0.28 | 3 | ||
| rs950776 | 1.000 | 0.080 | 15 | 78633676 | intron variant | T/C | snv | 0.26 | 3 | ||
| rs11072793 | 1.000 | 0.080 | 15 | 78714100 | intron variant | G/A | snv | 0.58 | 2 | ||
| rs121913316 | 1.000 | 0.080 | 19 | 1220489 | missense variant | A/T | snv | 2 | |||
| rs4539564 | 1.000 | 0.080 | 15 | 78836157 | intron variant | G/A | snv | 0.55 | 2 | ||
| rs761896295 | 1.000 | 0.080 | 4 | 1804450 | missense variant | G/A | snv | 2.4E-05 | 2.1E-05 | 2 | |
| rs863224682 | 1.000 | 0.080 | 17 | 7669655 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
| rs11090598 | 1.000 | 0.080 | 22 | 30125781 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs116895242 | 1.000 | 0.080 | 7 | 124306349 | intron variant | T/A | snv | 2.6E-02 | 1 | ||
| rs12167333 | 1.000 | 0.080 | 22 | 30179823 | downstream gene variant | C/T | snv | 0.21 | 1 | ||
| rs12446308 | 1.000 | 0.080 | 16 | 6367932 | intron variant | A/G | snv | 8.8E-02 | 1 | ||
| rs1245371 | 1.000 | 0.080 | 6 | 30070575 | 3 prime UTR variant | A/G | snv | 0.23 | 1 | ||
| rs142771326 | 1.000 | 0.080 | 11 | 111766340 | missense variant | C/G;T | snv | 2.0E-04 | 5.2E-04 | 1 | |
| rs1446876735 | 1.000 | 0.080 | 3 | 10142164 | missense variant | G/A | snv | 1 | |||
| rs1655902 | 1.000 | 0.080 | 6 | 29949078 | downstream gene variant | G/A;C | snv | 1 | |||
| rs193473 | 1.000 | 0.080 | 22 | 30052410 | intron variant | A/G;T | snv | 1 | |||
| rs1978083 | 1.000 | 0.080 | 22 | 30174454 | intron variant | C/G | snv | 0.21 | 1 | ||
| rs200426271 | 1.000 | 0.080 | 22 | 29948468 | intron variant | -/G | ins | 1 | |||
| rs2017677 | 1.000 | 0.080 | 22 | 29987273 | non coding transcript exon variant | G/C;T | snv | 1 | |||
| rs2023683 | 1.000 | 0.080 | 22 | 30203607 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs2412963 | 1.000 | 0.080 | 22 | 29995292 | non coding transcript exon variant | G/A | snv | 0.74 | 1 | ||
| rs2508049 | 1.000 | 0.080 | 6 | 29856106 | intron variant | A/G | snv | 0.11 | 1 |