| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 35 | ||
| rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 5 | |||
| rs260020 | 1.000 | 0.040 | 20 | 59138970 | intron variant | C/T | snv | 0.20 | 1 | ||
| rs35879803 | 1.000 | 0.040 | 4 | 145861685 | non coding transcript exon variant | C/A;T | snv | 1 | |||
| rs4345206 | 1.000 | 0.040 | 4 | 145845384 | intron variant | T/C | snv | 0.59 | 1 | ||
| rs16948048 | 0.925 | 0.040 | 17 | 49363104 | intron variant | A/G | snv | 0.37 | 5 | ||
| rs62076439 | 1.000 | 0.040 | 17 | 49327266 | intron variant | G/A;T | snv | 1 | |||
| rs3827066 | 0.925 | 0.040 | 20 | 45957384 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs6102343 | 1.000 | 0.040 | 20 | 41295639 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs2342781 | 1.000 | 0.040 | 8 | 105253492 | intron variant | C/G;T | snv | 1 | |||
| rs2106261 | 0.763 | 0.160 | 16 | 73017721 | intron variant | C/G;T | snv | 1 | |||
| rs6740731 | 1.000 | 0.040 | 2 | 144513025 | 3 prime UTR variant | G/A;C;T | snv | 0.25 | 1 | ||
| rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 13 | ||
| rs4739066 | 0.925 | 0.080 | 8 | 63191534 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs7819412 | 0.827 | 0.120 | 8 | 11187652 | intron variant | G/A;T | snv | 1 | |||
| rs6725887 | 0.851 | 0.080 | 2 | 202881162 | intron variant | T/C | snv | 8.9E-02 | 2 | ||
| rs6728861 | 1.000 | 0.040 | 2 | 203009020 | intron variant | G/A | snv | 9.0E-02 | 1 | ||
| rs1063856 | 0.763 | 0.400 | 12 | 6044368 | missense variant | T/C;G | snv | 0.31 | 2 | ||
| rs216311 | 0.882 | 0.040 | 12 | 6019277 | missense variant | T/A;C | snv | 4.0E-06; 0.69 | 2 | ||
| rs1185460 | 1.000 | 0.040 | 11 | 119072723 | non coding transcript exon variant | A/G | snv | 0.48 | 1 | ||
| rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 1 | ||
| rs9912587 | 1.000 | 0.040 | 17 | 43021069 | intron variant | G/A | snv | 0.28 | 1 | ||
| rs1561198 | 0.882 | 0.120 | 2 | 85582866 | upstream gene variant | C/T | snv | 0.52 | 1 | ||
| rs2516839 | 0.732 | 0.320 | 1 | 161043331 | 5 prime UTR variant | C/T | snv | 0.49 | 1 | ||
| rs3775058 | 1.000 | 0.040 | 4 | 95196220 | intron variant | A/T | snv | 0.75 | 1 |