| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3740058 | 1.000 | 0.080 | 10 | 99896225 | intron variant | G/A | snv | 0.34 | 0.31 | 1 | |
| rs11190305 | 1.000 | 0.080 | 10 | 99880120 | missense variant | A/C;G | snv | 0.34; 8.0E-06 | 1 | ||
| rs3740066 | 0.724 | 0.440 | 10 | 99844450 | missense variant | C/G;T | snv | 2.4E-05; 0.34 | 20 | ||
| rs4900442 | 1.000 | 0.080 | 14 | 99691904 | intron variant | C/T | snv | 0.47 | 0.43 | 1 | |
| rs754203 | 0.807 | 0.200 | 14 | 99691630 | non coding transcript exon variant | A/G | snv | 0.27 | 6 | ||
| rs7157609 | 1.000 | 0.080 | 14 | 99684108 | upstream gene variant | G/A | snv | 0.27 | 1 | ||
| rs3783320 | 1.000 | 0.080 | 14 | 99683121 | upstream gene variant | A/G;T | snv | 1 | |||
| rs8003602 | 0.925 | 0.120 | 14 | 99682624 | upstream gene variant | T/C | snv | 0.67 | 2 | ||
| rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
| rs143083071 | 1.000 | 0.080 | 1 | 99242198 | intron variant | G/A | snv | 3.1E-03 | 1 | ||
| rs531564 | 0.672 | 0.480 | 8 | 9903189 | non coding transcript exon variant | G/C | snv | 0.14 | 27 | ||
| rs115809613 | 1.000 | 0.080 | 4 | 98971324 | intron variant | A/G | snv | 4.8E-03 | 1 | ||
| rs7396366 | 0.925 | 0.120 | 11 | 986185 | intron variant | C/A | snv | 0.58 | 2 | ||
| rs117908734 | 1.000 | 0.080 | 14 | 98492717 | upstream gene variant | C/T | snv | 8.1E-03 | 1 | ||
| rs145364430 | 1.000 | 0.080 | 10 | 98429850 | missense variant | C/A;T | snv | 1.2E-05; 4.8E-05 | 1 | ||
| rs770299394 | 1.000 | 0.080 | 10 | 98425852 | missense variant | A/G | snv | 1 | |||
| rs113962169 | 1.000 | 0.080 | 10 | 98425662 | missense variant | A/G | snv | 1 | |||
| rs531454442 | 1.000 | 0.080 | 10 | 98425608 | missense variant | G/A | snv | 4.0E-05 | 1 | ||
| rs2233679 | 0.763 | 0.360 | 19 | 9834678 | splice region variant | C/T | snv | 0.59 | 11 | ||
| rs2233678 | 0.732 | 0.360 | 19 | 9834503 | non coding transcript exon variant | G/A;C | snv | 14 | |||
| rs2287839 | 1.000 | 0.080 | 19 | 9830138 | upstream gene variant | C/G | snv | 0.14 | 1 | ||
| rs6491411 | 1.000 | 0.080 | 13 | 98252314 | intron variant | T/A | snv | 0.87 | 1 | ||
| rs12378800 | 1.000 | 0.080 | 9 | 97869538 | regulatory region variant | G/A;T | snv | 1 | |||
| rs6714710 | 0.925 | 0.080 | 2 | 97728623 | intron variant | T/G | snv | 0.52 | 2 | ||
| rs1408585874 | 1.000 | 0.080 | 3 | 9757233 | missense variant | A/C | snv | 4.0E-06 | 1 |